204
LGC Standards Pharmacopoeial reference standards 2014 LGC Quality – ISO Guide 34 • GMP/GLP • ISO 9001 • ISO/IEC 17025 • ISO/IEC 17043 FOR STANDARDS WITH CofA SEE OUR CATALOGUE: PHARMACEUTICAL IMPURITIES AND PRIMARY REFERENCE STANDARDS WITH LINKS TO ALL WEBSHOP PRODUCTS

LGC Standards Pharmacopoeial reference standards 2014lgc.altey.kz/pdf/Pharmacopoeial_standards_2014.pdf · 2016-11-22 · e MM1172.00 drochloride 0 A 250mg HCl O N O A e MM0614.00

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  • LGC StandardsPharmacopoeial reference standards 2014

    LGC Quality – ISO Guide 34 • GMP/GLP • ISO 9001 • ISO/IEC 17025 • ISO/IEC 17043

    For standards with Cofa see our CataLoGue: PharmaCeutiCaL imPurities and Primary reFerenCe standards

    with L

    inks t

    o aLL

    websh

    oP Pro

    duCts

  • CAS No. CS Price Unit

    Product

    Code

    Pharmaceutical impurities

    Adiphenine HydrochlorideMM1172.00 Adiphenine Hydrochloride

    50-42-0A 250mg

    HCl

    O N

    O

    Adrenaline TartrateMM0614.00 Adrenaline Tartrate

    51-42-3A 500mg

    O

    O

    OHOH

    OHOH

    OHNH

    OH

    OH

    MM0614.02 L-Adrenaline

    51-43-4A 500mg

    NH

    OH

    OH

    OH

    MM0614.13Imp. C (EP) as Hydrochloride: 1-(3,4-Di-

    hydroxyphenyl)-2-(methylamino)ethanone

    Hydrochloride (Adrenalone Hydrochloride) 62-13-5A 100mg

    HClNH

    O

    OH

    OH

    MM0614.01(1R)-1-(3,4-Dihydroxyphenyl)-2-methylaminoethanesulphonic Acid(Adrenaline -Sulphonate)

    78995-75-2A 100mg S

    OHO OOH

    NH

    OH

    Alanine

    MM0566.00 Alanine

    56-41-7A 500mg

    N H 2

    OH

    O

    MM0567.00 Imp. A (Pharmeuropa): (2S)-2-Aminobutanedioic Acid

    (Aspartic Acid)

    56-84-8A 500mg

    OH

    O N H2

    OH

    O

    AlbendazoleMM0382.00 Albendazole

    54965-21-8A 500mg

    S

    NH

    NNH

    O

    O

    MM0382.01 Imp. A (EP): 5-(Propylsulphanyl)-1H-benzimidazol-2-amine

    80983-36-4A 100mg

    S

    NH

    NN H 2

    MM0382.02 Imp. B (EP): Methyl [5-Propylsulphinyl)-1H-benzimidazol-2-yl]carbamate

    54029-12-8A 100mg

    S

    O

    NH

    NNH

    O

    O

    MM0382.03 Imp. C (EP): Methyl [5-Propylsulphonyl)-

    1H-benzimidazol-2-yl]carbamate75184-71-3

    A 100mgS

    OO

    NH

    NNH

    O

    O

    MM0382.04 Imp. D (EP): 5-(Propylsulphonyl) -1H-benzimidazol-2-amine

    80983-34-2A 100mg

    SOO

    NH

    NN H2

    MM2500.00 Imp. E (EP): Methyl (1H-Benzimidazol-2-

    yl)carbamate (Carbendazim)

    10605-21-7A 100mg NH

    NNH

    O

    O

    Alfuzosin HydrochlorideMM0085.04 Imp. B (EP): 2-Chloro-6,7-dimethoxyquinazolin-

    4-amine

    23680-84-4A 100mg N

    N

    N H 2

    Cl

    O

    O

    MM1004.04Imp. D (EP) as Dihydrochloride: N-(4-Amino-6,7-

    dimethoxyquinazolin-2-yl)-N-methylpropane-1,3-

    diamine Dihydrochloride

    n/aA 50mg

    2

    HCl

    N

    N

    N H 2

    NN H 2O

    O

    Visit us at www.lgcstandards.com

    6

    Print_LGC_Katalog_MM_2013-11-27_NoHyperlink_v04j.pdf 6

    20/01/2014 15:55:39

    LGC StandardsPharmaceutical im

    purities and

    primary reference standards 2014

    LGC Quality – ISO Guide 34

    • GMP/GLP • ISO 9001 • ISO

    /IEC 17025 • ISO/IEC 17043

    LGC Quality - ISO Guide 34 • GMP/GLP • ISO 9001 • ISO/IEC 17025 • ISO/IEC 17043

    Visit us at www.lgcstandards.com @LGCStdsPharma

    Also available from LGC Standards: ‘Pharmaceutical impurities and primary reference standards 2014’

    A comprehensive catalogue of more than 3,000 pharmaceutical impurities and primary reference standards manufactured by LGC.

    Contact your local LGC Standards office for your free copy, or download a PDF version of this catalogue at www.lgcstandards.com.

    Request your copy now!

    © LGC Limited, 2014. All rights reserved. LGC Standards is part of the LGC Group. 3970/LB/0514

  • Introduction

    www.lgcstandards.com@LGCStdsPharma

    With links to all

    Webshop products

  • LGC Quality - ISO Guide 34 • GMP/GLP • ISO 9001 • ISO/IEC 17025 • ISO/IEC 17043

    © LGC Limited, 2013. All rights reserved. LGC Standards is part of the LGC Group. 3664/LB/0713

    Our website offers the most comprehensive source of reference materials - now available for ONLINE ordering.

    Anyone can browse product information online, simply visit: www.lgcstandards.com

    To view pricing and to place an order, please register at: www.lgcstandards.com/register

    For further information visit www.lgcstandards.com or contact your local office.

    56,000referencematerials

    yourstandard+ =oneintuitivesearch engine

    Buy pharmaceutical reference materials online

    3677_standards_webshop_ad_v4.indd 1 1/14/2014 5:40:43 PM

  • 5Email: [email protected] | Website: www.lgcstandards.com

    Contents

    Introduction ���������������������������������������������������������������������������������������������������������������������������������������� 6

    European Pharmacopoeia ��������������������������������������������������������������������������������������������������������������� 11

    United States Pharmacopoeia ��������������������������������������������������������������������������������������������������������� 77

    British Pharmacopoeia and others ����������������������������������������������������������������������������������������������� 161

    Complementary products ������������������������������������������������������������������������������������������������������������� 189

    3970_1Pharma_catalogue_internal_pages_v2.indd 5 6/12/2014 12:04:33 PM

  • 6 Email: [email protected] | Website: www.lgcstandards.com

    IntroductionWelcome to the new edition of our pharmacopoeial reference standards catalogue�

    About LGC Standards

    LGC Standards has successfully established a global reputation for the production of impurities and working standards, and as a single source for the supply of pharmacopeia reference materials� Our menu of custom services, including custom synthesis of impurities and metabolites, characterisation, certification, packaging and distribution, adds value to the scientific support we provide to our pharmaceutical customers�

    Our relationships with the world’s leading pharmacopoeias and their range of Chemical Reference Substances (CRS) and Reference Standards (RS), combined with in-house production of primary reference standards and pharmaceutical impurities, enable us to meet our customers’ specific needs. LGC Standards is also the exclusive European distributor for ATCC cultures and bio products�

    LGC Standards’ extensive network of sales offices and distribution centres means we offer the widest range of reference materials from one single source for rapid delivery� Our staff can provide scientific and technical guidance, including shipping and customs advice, in the local language.

    Our range of products also includes reference materials for clinical and forensic applications, phytochemicals, environmental analysis, physical properties determination, and food and beverage analysis�

    For more information about our range of services, or to receive any of our catalogues, please refer to our website www�lgcstandards�com or contact your local office.

    About LGC

    LGC is an international life sciences measurement and testing company, which builds upon leading positions in sustainably growing markets. LGC provides reference materials, proficiency testing, genomics and analytical products and services which underpin the safety, health and security of the public to customers in the Pharmaceutical, Agricultural Bioscience, Food and Environment, Government and Academia, Security and Sports markets.

    With headquarters in Teddington, South West London, LGC employs over 2,000 staff, operating out of 22 countries worldwide. Its operations are extensively accredited to international quality standards such as ISO/IEC 17025 and ISO Guide 34.

    With a history dating back to 1842, LGC has been home to the UK Government Chemist for more than 100 years. It is the designated UK National Measurement Institute for Chemical and Bioanalytical measurement, providing metrology research, calibration and testing� LGC was privatised in 1996 and is now majority-owned by funds managed by Bridgepoint�

    For more information, please visit www�lgcgroup�com

    3970_1Pharma_catalogue_internal_pages_v2.indd 6 6/12/2014 12:04:33 PM

  • 7Email: [email protected] | Website: www.lgcstandards.com

    About the catalogue

    This catalogue comprises the reference standards from the major pharmacopoeias, plus ready to use reagents as they are outlined in the chapters 2 and 4 of the European Pharmacopoeia and further complementary products�

    For our own range of primary and impurity reference standards, please refer to the current catalogue “Pharmaceutical impurities and primary reference standards”. It is also available for download from our website.

    The information provided in this catalogue as regards compendial articles is based on the ‘official’ pharmacopoeial lists and is correct at the time of print� Original descriptions and spellings used by the producers are retained�

    Pharmaceutical reference substances

    Certification

    The products described in this catalogue include pharmacopeial reference substances for use in pharmaceutical analysis. Pharmacopeial CRS and RS should be distinguished from certified reference materials (CRM), which are produced in conformity with the ISO guides 30 to 35, and supplied with a detailed certification document.

    Pharmacopeial reference substances are produced for a specific purpose, and the manufacturers follow rigorous protocols to ensure the reference substance is fit for the intended purpose. The ‘certification’ processes follow the basic requirements of the relevant ISO REMCO guides, but are modified by the pharmacopoeias to reflect the particular demands of the associated pharmacopeial monograph�

    Details are given in the introduction to each section listing the various CRS/RS collections in this catalogue�

    Shelf life, storage, expiry dates and unit sizes

    Pharmacopeial CRS and RS should be purchased when required and not stored for a prolonged period�

    Pack sizes are designed to allow a limited number of replicate analyses, as required by Good Analytical Practice, but the opened pack should not be kept for future use. Please check all individual storage temperature requirements and note that the substances should be kept away from humidity and light (unless otherwise stated)�

    Specific lot numbers or letters are allocated to all pharmacopeial reference substances, but no expiry dates are set. New lots are normally prepared well in advance of the expected ‘sell-out’ of the current lot�

    Please note that new lots can have different unit sizes, especially with pharmacopoeial reference standards, and LGC Standards is not responsible for such cases. If the unit size of a new batch changes, LGC Standards will provide this information to customers in new lot lists.

    When a certain batch of a CRS/RS is withdrawn from sale because the lot has depleted a final expiry date is given, by which any material of the expiring lot held by users must be used. Parallel to that the new lot comes into distribution. This means that for a period of time both expiring and new lot are ‘official’. Lot information is available from LGC Standards.

    3970_1Pharma_catalogue_internal_pages_v2.indd 7 6/12/2014 12:04:33 PM

  • 8 Email: [email protected] | Website: www.lgcstandards.com

    If a material is withdrawn by the producer, then all stocks held by the users are no longer valid and expire immediately. Should this occur, LGC Standards will inform all customers who have purchased the withdrawn substance recently from LGC Standards� Please note that such a situation is outside LGC Standards’ control and products are not refundable�

    Once opened, the pharmacopoeias can no longer guarantee the stability of the material and any of the CRS/BRP and RS not used should be disposed of and not kept for future use�

    Impurity standards

    Impurities in a pharmaceutical substance can change the effects and side effects of a drug significantly. Therefore, it is important to have an accurate detection of impurities. The pharmaceutical monographs regulate the legal definition, the analysis and the limits of impurities of a given substance. An official but limited range of impurity standards is available from the main pharmacopoeias where required in the monograph�

    Approximately 3,000 other impurity standards are listed in the catalogue ‘Pharmaceutical impurities and primary reference standards’ which has been published separately and is available via your local LGC Standards office or via download from our website.

    These materials are produced at our facility in Luckenwalde near Berlin, Germany, and are supplied with a full certificate of analysis. Our impurity reference standards are intended for the identification and control of impurities in drug substances and drug preparations, as well as for method development and validation�

    Controlled substances

    A number of the pharmaceutical substances, such as narcotics and tranquillisers, described in this catalogue are so called controlled substances�

    The purchase, possession and use of controlled substances are subject to national and international regulations designed to limit their abuse� It is the responsibility of the customer to obtain any authorisation necessary to both purchase and possess controlled substances, complying with the laws of the importing country, before ordering�

    Customers wishing to obtain controlled substances must contact their LGC Standards sales office before ordering, and clarify with the sales specialists the relevant national requirements, the associated charges and consequential delivery times. All orders for controlled substances must be provided in writing and signed by an authorised person. The orders must be accompanied with the original import permit and/or possession permit�

    3970_1Pharma_catalogue_internal_pages_v2.indd 8 6/12/2014 12:04:33 PM

  • 9Email: [email protected] | Website: www.lgcstandards.com

    Use, safety and handling

    Please read any documents supplied with the product before opening or using it� Particular attention must be paid to instructions referring to pre-mixing, addition of diluent to lyophilised materials and to the minimum size of sample to be used. The latter point is particularly important as it has normally been set by the producer after considering fully the homogeneity testing data obtained as a part of the certification exercise. The use of smaller than recommended samples is one of the most common sources of error�

    Some pharmaceutical substances are toxic and require special handling. Virtually all pharmaceutical reference substances have a pharmacological and/or biological activity� We therefore recommend that all the products described in this catalogue should be handled as if they were bio-active, toxic or infective, and that opened packs should only be handled by trained laboratory personnel� We also strongly recommend to read the information provided by material safety data sheets coming with the products�

    All pharmaceutical reference substances and standards are for laboratory analytical use only and not for use in humans.

    General ordering information

    Prices and delivery procedures are available from your local LGC Standards office. For products requiring special delivery procedures (cooled shipping, special licensing, controlled substances) additional charges may be applied�

    Please note that once delivered to the customer, reference substances are not returnable�

    Customers requiring assistance with the purchase, use or application of a particular reference substance should contact LGC Standards where technical staff are available to advise on the use and suitability of the products�

    3970_1Pharma_catalogue_internal_pages_v2.indd 9 6/12/2014 12:04:33 PM

  • 10 Email: [email protected] | Website: www.lgcstandards.com

    Notes

    3970_1Pharma_catalogue_internal_pages_v2.indd 10 6/12/2014 12:04:33 PM

  • European Pharmacopoeia

    www.lgcstandards.com@LGCStdsPharma

    With links to all

    Webshop products

  • LGC Quality - ISO Guide 34 • GMP/GLP • ISO 9001 • ISO/IEC 17025 • ISO/IEC 17043

    LGC Standards custom synthesis can provide you with research material for nearly every pharmaceutical impurity you want!

    LGC Standards custom synthesis is a special service to customers who need a specific standard which is not available in our catalogue range. All kinds of standards are possible – from ordinary pharmacopoeial impurities to stable-isotope-labelled metabolites – with the desired purity and characterisation, in batch scales from milligramme to kilogramme.

    Visit us at www.lgcstandards.com

    Looking for the one impurity?LGC Standards custom synthesis

    © LGC Limited, 2013. All rights reserved. LGC Standards is part of the LGC Group. 3664/LB/0713

    3677_pharma_custom_syn_ad_v4.indd 1 1/14/2014 11:20:56 AM

  • 13Email: [email protected] | Website: www.lgcstandards.com

    Introduction

    European Pharmacopoeia (EP) (from page 15)

    Background

    European Pharmacopoeia reference substances and preparations are selected and verified by the EP laboratories as being suitable for the use as prescribed in the relevant monograph of the European Pharmacopoeia.

    Any reference substance, spectra or preparation required for a new EP monograph, shall be available as soon as the monograph comes into force.

    Since chemical reference substances (CRS) and biological reference preparations (BRP) are officially certified by the European Pharmacopoeia Commission, it should be noted that neither certificates of analysis nor data not relevant to the use of the products as defined by the EP monograph are provided with the reference product or substance.

    Relationship with other pharmacopoeias in Europe

    Many of the member countries of the European Pharmacopoeia Commission have adopted the EP in full, and their monographs require only EP CRS/BRP. When an EP monograph is adopted by the pharmacopoeia of a member state of the Council of Europe then any reference material that may have been available from a national pharmacopoeia, e.g. BP or PF, will usually be discontinued in favour of the EP reference substance. However, a number of member countries of the EP Commission maintain national pharmacopoeial monographs, especially for finished dosage forms, which require the use of separate reference substances.

    A separate chapter in this catalogue includes lists of the reference substances produced for the British, French and International pharmacopoeia monographs. The International Pharmacopoeia (IP) reference substances are described in the section referring to the WHO (World Health Organization).

    Storage, shelf life, expiry dates and size units

    European Pharmacopoeia CRS/BRP are subject to regular inspection and repeated analysis by EP scientific staff. Each EP CRS/BRP is, on receipt by the customer, fit for the intended use.

    No expiry date is indicated on the reference materials because the products or substances comply with the requirements of the corresponding monograph and are monitored regularly. When batches are to be changed, LGC Standards can provide you with the date on which the previous lot will no longer be official.

    In specific cases for reasons related to filling or labeling, sub-batches are obtained from the same batch of bulk material. However, all the necessary precautions are taken in order to guarantee that the quality and specifications of the sub-batches do not differ from one to another.

    Please note, that new lots can have different unit sizes, especially with pharmacopoeial reference standards, and LGC Standards is not responsible for such cases. If the unit size of a new batch changes, LGC Standards will provide this information to customers in new lot lists.

    EP recommends only sufficient material should be purchased for immediate use and that unopened vials should be stored in the dark unless otherwise stated. Whilst most EP CRS/BRP can be shipped at ambient temperature, certain items have to be maintained at controlled temperatures at all times and are subject to special shipping charges and storage conditions (details are available on request).

    3970_2Pharma_catalogue_internal_EU_pharma_v1.indd 13 6/12/2014 3:33:20 PM

  • 14 Email: [email protected] | Website: www.lgcstandards.com

    Where no drying conditions are stated, the substance is to be used as received.

    Once opened, EP can no longer guarantee the stability of the CRS/BRP, and any material not used should be disposed of and not kept for future use.

    Validation of secondary standards

    All secondary in-house working standards have to be validated against the corresponding EP CRS/BRP.

    Please make sure that the secondary material is used only for the same official purposes for which the primary pharmacopoeial material was designed.

    Proper use

    For information on the use of the substances please refer to the monograph and leaflets accompanying the material, or contact your local LGC Standards office.

    Toxicity

    The potential toxicity of certain reference substances is such that special precautions should be taken to avoid contact.

    Such substances should be manipulated in a glove box. If this is not possible, gloves, eye protection and a mask should be worn.

    Following the guidelines suggested by the EP does not replace the need to carry out a full hazard assessment.

    Biological and blood products should be regarded as potentially hazardous to health and therefore used and disposed of according to established laboratory safety procedures.

    Controlled substances

    The EP product range contains substances subject to controlled substance regulations schedules. Special ordering procedures apply, so please contact LGC Standards for details and costs.

    3970_2Pharma_catalogue_internal_EU_pharma_v1.indd 14 6/12/2014 3:33:20 PM

  • European Pharmacopoeia

    Edition 2014 Visit us at www.lgcstandards.com 15

    European Pharmacopoeia standards Code Product Unit

    EPY0000053 17 alpha-dihydroequilin 10 mg EPY0000173 4-Aminobenzoic acid 60 mg EPA0460000 7-Aminodesacetoxycephalosporanic acid 20 mg EPY0001552 Abacavir for peak identification 10 mg EPY0001551 Abacavir for system suitability 10 mg EPY0001561 Abacavir sulfate 20 mg EPY0000055 Acamprosate calcium - Reference Spectrum unit

    EPY0000116 Acamprosate impurity A 3-aminopropane-1-sulphonic acid

    50 mg

    EPY0000500 Acarbose 94.7 mg EPY0000354 Acarbose for identification 10 mg EPY0000427 Acarbose for peak identification 20 mg EPA0040000 Acebutolol hydrochloride 50 mg

    EPY0000359

    Acebutolol impurity B N-[3-acetyl-4-[(2RS)-2-hydroxy-3-[(1-methylethyl) amino]propoxy]phenyl]acetamide (diacetolol)

    10 mg

    EPY0000127

    Acebutolol impurity C N-(3-acetyl-4-hydroxyphenyl)butanamide

    20 mg

    EPY0000128

    Acebutolol impurity I N-[3-acetyl-4-[(2RS)-3-(ethylamino)-2-hydroxypropoxy]phenyl)butanamide

    0.004 mg

    EPY0000056 Aceclofenac - Reference Spectrum unit EPY0001094 Aceclofenac for peak identification 10 mg

    EPY0000085 Aceclofenac impurity F benzyl [[[2-[(2,6-dichlorophenyl)amino]phenyl]acetyl]oxy]acetate

    20 mg

    EPY0000086

    Aceclofenac impurity H [[[[[[[2-[(2,6-dichlorophenyl)amino]phenyl]acetyl]oxy]acetyl]oxy]acetyl]oxy]acetic acid

    10 mg

    EPY0000810 Acemetacin 100 mg

    EPY0000811 Acemetacin impurity A 4-chlorobenzoic acid

    10 mg

    EPY0000842 Acemetacine impurity mixture 0.06 mg EPA0070000 Acesulfame potassium 50 mg

    EPA0070020 Acesulfame potassium impurity B 5-chloro-6-methyl-1,2,3-oxathiazin-4(3H)-one 2,2-dioxide

    50 mg

    EPA0100000 Acetazolamide 100 mg EPY0001084 Acetazolamide for system suitability 0.0068 mg EPY0000002 Acetylcholine chloride 50 mg EPA0150000 Acetylcysteine 50 mg

    EPA0152000 Acetylcysteine impurity C N,N'-diacetyl-L-cystine

    10 mg

    EPA0153000

    Acetylcysteine impurity D N,S-diacetyl-L-cysteine

    10 mg

    EPA0200000 Acetylsalicylic acid 15 mg EPY0001460 Acetylsalicylic acid for peak identification (10.26 mg) 10 mg EPY0001462 Acetylsulfadiazine 0.002 mg EPA0220000 Aciclovir 75 mg EPY0001271 Aciclovir for peak identification 1 0.3 mg EPY0001269 Aciclovir for peak identification 2 0.004 mg EPY0001264 Aciclovir for system suitability 10 mg EPA0225000 Acitretin 100 mg EPY0001543 Actaea racemosa for assay CRS 300 mg EPY0001463 Actaea racemosa HRS 1200 mg EPY0001464 Actaea rasemosa dry extract for system suitability HRS 1200 mg EPY0001121 Adapalene 100 mg

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  • European Pharmacopoeia

    16 Visit us at www.lgcstandards.com Edition 2014

    Code Product Unit

    EPY0001119 Adapalene for peak identification 2.022 mg

    EPY0001120 Adapalene impurity C 1-[2-(methyloxy)phenyl]tricyclo[3.3.1.1]decane

    6 mg

    EPA0230000 Adenine 50 mg EPA0230200 Adenosine 50 mg EPY0000110 Adipic acid 50 mg EPY0000882 Adrenaline 5 mg EPY0000740 Adrenaline impurity mixture 0.005 mg EPA0300000 Adrenaline tartrate 100 mg EPY0000707 Adrenaline tartrate with impurity A 15 mg EPY0000883 Adrenaline with impurity F 10 mg EPY0000728 Agnus castus fruit standardised dry extract 200 mg EPA0325000 Alanine 60 mg EPA0325100 Albendazole 50 mg EPA0325200 Alcuronium chloride 50 mg EPA0325450 Alfacalcidol 5 mg EPA0325451 Alfacalcidol - Reference Spectrum unit EPY0001601 Alfacalcidol for system suitability 2.5 mg EPA1225000 Alfadex 150 mg EPA0325500 Alfentanil hydrochloride - Reference Spectrum unit EPY0000832 Alfuzosin for system suitability 10 mg EPA0325800 Alfuzosin hydrochloride 10 mg EPY0001581 Alimemazine for system suitability 5 mg EPY0001583 Alimemazine hemitartrate 15 mg EPA0349000 Allantoin 60 mg EPA0350000 Allopurinol 100 mg

    EPA0350010 Allopurinol impurity A 5-amino-1H-pyrazole-4-carboxamide

    10 mg

    EPA0350020

    Allopurinol impurity B 5-formylamino-1H-pyrazole-4-carboxamide

    10 mg

    EPA0350030

    Allopurinol impurity C 5-(4H-1,2,4-triazol-4-yl)1H-pyrazole-4-carboxamide

    10 mg

    EPA0350040

    Allopurinol impurity D ethyl 5-amino-1H-pyrazole-4-carboxylate

    15 mg

    EPA0350050

    Allopurinol impurity E ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate

    20 mg

    EPY0000383 All-rac-alpha-tocopherol for peak identification 50 mg EPY0000384 All-rac-alpha-tocopheryl acetate for peak identification 30 mg EPA0351000 Allylstrychnine bromide 10 mg EPY0000235 Almagate 25 mg EPY0000255 Almagate - Reference Spectrum unit EPA1220000 Alpha-apo-oxytetracycline 20 mg EPT1550000 alpha-Tocopherol 500 mg EPT1600000 alpha-Tocopheryl acetate 500 mg EPA0357000 Alprazolam 100 mg EPA0360000 Alprenolol hydrochloride 100 mg EPY0000054 Alprostadil 50 mg EPY0000606 Altizide 150 mg

    EPY0000843 Altizide impurity B 3-[(2,2-dimethoxyethyl)sulphanyl]prop-1-ene

    15 mg

    EPY0000687 Alverine citrate 5 mg EPY0000595 Alverine for peak identification 0.125 mg

    EPY0000607 Alverine impurity D N-(3-cyclohexylpropyl)-N-ethyl-3-phenylpropan-1-amine

    10 mg

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  • European Pharmacopoeia

    Edition 2014 Visit us at www.lgcstandards.com 17

    Code Product Unit

    EPA0363000 Amantadine hydrochloride 100 mg EPA0363700 Ambroxol hydrochloride 125 mg EPA0900000 Amfetamine sulfate - Reference Spectrum unit EPA0365000 Amidotrizoic acid dihydrate 100 mg EPY0001461 Amidotrizoic acid for system suitability 0.08 mg EPA0368000 Amikacin 200 mg EPY0001117 Amikacin for system suitability 10 mg

    EPY0001467 Amikacin impurity I (2S)-4-amino-2-hydroxybutanoic acid

    20 mg

    EPA0365900 Amikacin sulfate 200 mg EPA0370000 Amiloride hydrochloride 100 mg

    EPY0000020 Amiloride impurity A methyl-3,5-diamino-6-chloropyrazine-2-carboxylate

    20 mg

    EPA0420000 Aminocaproic acid 50 mg EPA0496000 Aminoglutethimide 125 mg

    EPA0496005

    Aminoglutethimide impurity A (3RS)-3-(3-aminophenyl)-3-ethylpiperidine-2,6-dione; (3-aminoglutethimide)

    20 mg

    EPA0496020

    Aminoglutethimide impurity D 3,3'-[diazenediyldi(4,1-phenylene)]bis(3-ethylpiperidine-2,6-dione) (azoglutethimide)

    10 mg

    EPA0575000 Amiodarone hydrochloride 100 mg

    EPY0000129 Amiodarone impurity D (2-butyl-benzofuran-3-yl)-(4-hydroxy-3,5-diiodophenyl)methanone

    20 mg

    EPY0000130

    Amiodarone impurity E (2-butylbenzofuran-3-yl)(4-hydroxyphenyl)methanone

    20 mg

    EPA0590000 Amisulpride 10 mg EPY0001534 Amisulpride for system suitability (1.0015 mg) 1 mg EPY0000563 Amitriptyline hydrochloride 10 mg EPY0000049 Amlodipine besilate 150 mg EPY0001067 Amlodipine for peak identification 10 mg

    EPY0001068

    Amlodipine impurity A 3-ethyl 5-methyl (4RS)-4-(2-chlorophenyl)-2-[[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]methyl]-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate

    15 mg

    EPY0001069

    Amlodipine impurity B 3-ethyl 5-methyl (4RS)-4-(2-chlorophenyl)-6-methyl-2-[[2-[[2-(methylcarbamoyl)benzoyl]amino]ethoxy]methyl]-1,4-dihydropyridine-3,5-dicarboxylate

    15 mg

    EPY0001070

    Amlodipine impurity G dimethyl 4-(2-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

    15mg

    EPY0000302 Ammonio methacrylate copolymer (type A) - Reference Spectrum unit EPY0000303 Ammonio methacrylate copolymer (type B) - Reference Spectrum unit EPY0000433 Ammonium glycyrrhizate 70 mg EPA0650000 Amobarbital 500 mg EPA0700000 Amobarbital sodium 500 mg EPA0800000 Amoxicillin trihydrate 100 mg EPY0001521 Amoxicillin trihydrate for performance verification 5 g EPY0000005 Amphotericin B 100 mg EPY0001361 Amphotericin B for microbiological assay 100 mg EPY0001014 Amphotericin B for peak identification 10 mg EPA1000000 Ampicillin (anhydrous) 250 mg EPA1100000 Ampicillin trihydrate 150 mg EPY0001244 Amylmetacresol 285 mg EPY0001245 Amylmetacresol for peak identification 10 mg EPY0001522 Anastrozole 100 mg

    EPY0001531 Anastrozole impurity E 2,2'-[5-(hydroxymethyl)benzene-1,3-diyl]bis(2-methylpropanenitrile)

    10 mg

    EPY0001386 Angelica dahuria root 160 mg

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  • European Pharmacopoeia

    18 Visit us at www.lgcstandards.com Edition 2014

    Code Product Unit

    EPY0001385 Angelica pubescent root 500 mg EPA1200000 Anhydrotetracycline hydrochloride 15 mg EPY0001466 Anhydrous Docetaxel 15 mg EPA1210000 Antazoline hydrochloride 50 mg EPY0001465 Apomorphine hydrochloride hemihydrate 15 mg EPY0001471 Apomorphine impurity B (Morphine sulfate) (Morphinhemisulfat-Pentahemihydrat) 40 mg EPY0001154 Aprotinin for system suitability 2.7 mg EPA1250000 Aprotinin solution BRP 0.5 mL EPY0000806 Arbutin 100 mg EPA1270000 Arginine 50 mg EPY0000304 Arginine aspartate 20 mg EPA1271000 Arginine hydrochloride 60 mg EPY0001649 Aripiprazole 170 mg

    EPY0001650 Aripiprazole impurity F 7-[4-[4-(2,3-dichlorophenyl)-1-oxidopiperazin-1-yl]-3,4-dihydroquinolein-2(1H)-one

    10 mg

    EPY0001323 Aristolochia 140 mg EPY0001175 Aristolochic acid for system suitability 1 mg EPY0001185 Aristolochic acid I 11 mg EPY0000079 Articaine hydrochloride 100 mg

    EPY0000080 Articaine impurity A methyl3-[[2-(propylamino)acetyl]amino]-4-methylthiophene-2-carboxylate

    15 mg

    EPY0000081

    Articaine impurity E methyl 4-methyl-3-[[(2RS)-2-[(1-methylethyl)amino]propanoyl] amino]thiophene-2-carboxylate

    10 mg

    EPA1300000 Ascorbic acid (Vitamin C) 100 mg

    EPY0001024 Ascorbic acid impurity C D-sorbosonic acid

    20 mg

    EPY0001170

    Ascorbic acid impurity D methyl D-xylo-hex-2-ulosonate (methyl D-sorbosonate)

    10 mg

    EPY0000800 Ascorbyl palmitate 10 mg EPY0000305 Asparagine monohydrate 60 mg EPA1320000 Aspartame 40 mg

    EPA1321000 Aspartame impurity A 2-(5-benzyl-3,6-dioxopiperazin-2-yl)acetic acid (diketopiperazine)

    10 mg

    EPA1330000 Aspartic acid 50 mg EPY0001171 Astragaloside IV 40 mg EPA1340000 Atenolol 100 mg EPY0001089 Atenolol for system suitability 5 mg EPY0001587 Atomoxetine for impurity A identification 10 mg EPY0001586 Atomoxetine hydrochloride 110 mg

    EPY0001588 Atomoxetine impurity B (3S)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1- amine

    10 mg

    EPY0001589

    Atomoxetine impurity D (3R)-N-methyl-3-(3-methylphenoxy)-3-phenylpropan-1- amine

    5 mg

    EPY0001327 Atorvastatin calcium trihydrate 150 mg

    EPY0001328 Atorvastatin impurity A desfluoroatorvastatin

    10 mg

    EPY0001329

    Atorvastatin impurity B 3-epi-atorvastatin

    10 mg

    EPY0001330

    Atorvastatin impurity C fluoroatorvastatin

    10 mg

    EPY0001331

    Atorvastatin impurity D 3-[(4-fluorophenyl)carbonyl]-2-(2-methylpropanoyl)-N,3-diphenyloxirane-2-carboxamide

    10 mg

    EPY0001332

    Atorvastatin impurity E ent-atorvastatin

    10 mg

    EPY0001572 Atovaquone 270 mg

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  • European Pharmacopoeia

    Edition 2014 Visit us at www.lgcstandards.com 19

    Code Product Unit

    EPY0001573 Atovaquone for system suitability 10 mg EPY0000424 Atracurium besilate 120 mg EPY0000503 Atracurium for impurity F identification 5 mg EPY0000504 Atracurium for peak identification 5 mg EPY0000878 Atropine 30 mg EPY0000845 Atropine for peak identification 0.25 mg

    EPY0000816 Atropine impurity B (1R,3r,5S)-8-azabicyclo[3.2.1]oct-3-yl (2RS)-3-hydroxy-2-phenylpropanoate (noratropine)

    10mg

    EPA1400000 Atropine sulphate 50 mg EPY0000029 Azaperone 50 mg EPA1500000 Azathioprine 100 mg

    EPY0001240 Azathioprine impurity A 1-methyl-4-nitro-1H-imidazol-5-amine

    10 mg

    EPY0001246

    Azathioprine impurity G 6-[(1-methyl-4-nitro-1H-imidazol-5-yl)sulfanyl]-7H-purin-2-amine (thiamiprine)

    5 mg

    EPY0000326 Azelastine hydrochloride 25 mg

    EPY0000327 Azelastine impurity B 1-benzoyl-2-[(4RS)-1-methylhexahydro-1H-azepin-4-yl]diazane

    5 mg

    EPY0000328

    Azelastine impurity D 4-(4-chlorobenzyl)phthalazin-1(2H)-one

    5 mg

    EPY0000329

    Azelastine impurity E 3-(4-chlorobenzilidene)isobenzofuran-1(3H)-one

    5 mg

    EPY0000306 Azithromycin 200 mg EPY0000637 Azithromycin for peak identification 15 mg EPY0000641 Azithromycin for system suitability 0.05 mg

    EPY0000307 Azithromycin impurity A 6-demethylazithromycin

    10 mg

    EPB0070000 Bacampicillin hydrochloride 120 mg EPB0100000 Bacitracin zinc 150 mg EPB0200000 Baclofen 50 mg

    EPB0200050 Baclofen impurity A (RS)-4-amino-3-(4-chlorophenyl)butyric acid lactam

    50 mg

    EPY0001273 Baicalin 10 mg EPB0250000 Bambuterol hydrochloride 100 mg EPB0300000 Barbital 500 mg EPY0001525 Basic butylated methacrylate copolymer 20 mg EPY0000295 Basic butylated methacrylate copolymer - Reference Spectrum unit EPB0305000 Beclometasone dipropionate anhydrous 150 mg EPY0000469 Beclometasone dipropionate for peak identification 10 mg EPY0000352 Beclometasone dipropionate for system suitability 15 mg EPY0001073 Beclometasone dipropionate impurities F and N 0.052 mg EPY0000351 Beclometasone dipropionate monohydrate 10 mg EPY0001607 Belamcanda chinensis rhizome HRS 110 mg EPY0001038 Benazepril for system suitability 0.016 mg EPY0001025 Benazepril hydrochloride 160 mg

    EPY0001026

    Benazepril impurity A [(3R)-3-[[(1R)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid

    10 mg

    EPB0400000 Bendroflumethiazide 100 mg

    EPY0000564 Bendroflumethiazide impurity A 4-amino-6-(trifluoromethyl)benzene-1,3-disulphonamide

    5 mg

    EPB0470000 Benperidol 100 mg EPY0001079 Benserazide for peak identification 10 mg EPB0477000 Benserazide hydrochloride 50 mg

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  • European Pharmacopoeia

    20 Visit us at www.lgcstandards.com Edition 2014

    Code Product Unit

    EPB0477010

    Benserazide impurity A (RS)-2-amino-3-hydroxypropanohydrazide

    20 mg

    EPY0001071

    Benserazide impurity C (2RS)-2-amino-3-hydroxy-2'-[(1EZ)-(2,3,4-trihydroxybenzylidene)]propanohydrazide

    10 mg

    EPY0001064 Benzaldehyde 150 mg EPY0001060 Benzalkonium chloride for system suitability 20 mg

    EPB0490000 Benzarone (2-ethylbenzofuran-3-yl)(4-hydroxyphenyl)methanone

    10 mg

    EPB0500000 Benzathine benzylpenicillin 200 mg EPY0000775 Benzbromarone 10 mg EPB0550000 Benzethonium chloride 100 mg EPB0600000 Benzocaine 50 mg EPY0001470 Benzoic acid 30 mg EPY0000647 Benzophenone 40 mg EPY0000167 Benzyl alcohol 50 mg EPB0670000 Benzyl benzoate - Reference Spectrum unit EPB0700000 Benzylpenicillin potassium 100 mg EPB0900000 Benzylpenicillin sodium 200 mg EPY0001149 Berberine chloride 20 mg EPA1230000 Beta-apo-oxytetracycline 20 mg EPB0950000 Betadex 200 mg EPY0000391 Betahistine dihydrochloride 50 mg EPB0990000 Betahistine mesilate 100 mg EPB1000000 Betamethasone 75 mg EPB1030000 Betamethasone acetate 100 mg EPY0001416 Betamethasone dipropionate for peak identification 10 mg EPY0001418 Betamethasone dipropionate for system suitability 10 mg EPB1040000 Betamethasone diproprionate 150 mg EPB1045000 Betamethasone sodium phosphate 100 mg EPY0001027 Betamethasone valerate for system suitability 25 mg EPY0001065 Betamethasone valerate impurity mixture 0.018 mg EPB1054000 Betamethasone-17-valerate 100 mg EPB1055000 Betamethasone-21-valerate 15 mg EPY0001615 Beta-sitosterol 25 mg EPY0001360 Betaxolol for peak identification 15 mg EPB1103000 Betaxolol hydrochloride 60 mg

    EPB1103100 Betaxolol impurity A (2RS)-1-(4-ethylphenoxy)-3-[(1-methylethyl)-amino]propan-2-ol

    10 mg

    EPY0001354

    Betaxolol impurity C 2-[[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]methyl]oxirane

    5 mg

    EPB1115000 Bezafibrate 100 mg EPY0001444 Bicalutamide 100 mg EPY0001448 Bicalutamide for system suitability 15 mg EPY0001078 Bicisate labelling kit 24 mg EPB1110000 Bifonazole 100 mg EPY0001421 Bifonazole for system suitability 10 mg EPY0001059 Bilberry dry extract 250 mg EPB1116000 Biotin (Vitamin H) 20 mg EPB1120000 Biperiden hydrochloride 60 mg

    EPB1121000

    Biperiden impurity A (1RS)-1-[(1SR,2SR,4SR)-bicyclo[2.2.1]hept-5-en-2-yl]-1-phenyl-3-(piperidin-1-yl)propan-1-ol (endo form)

    20 mg

    EPB1140000 Bisacodyl 50 mg EPY0000608 Bisacodyl for peak identification 10 mg

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  • European Pharmacopoeia

    Edition 2014 Visit us at www.lgcstandards.com 21

    Code Product Unit

    EPY0000694 Bisacodyl for system suitability 5 mg

    EPY0000877

    Bisoprolol for peak identification Bisoprolol for system suitability method A CRS has been renamed as Bisoprolol for peak identification CRS

    1 mg

    EPY0000813

    Bisoprolol for system suitability Bisoprolol for system suitability method B CRS has been renamed as Bisoprolol for system suitability CRS

    1 mg

    EPY0000812 Bisoprolol fumarate 50 mg EPB1141000 Bleomycin sulfate 7 mg EPY0000434 Boldine 30 mg EPB1142000 Bordetella pertussis mouse antiserum BRP 0.5 mg EPY0001634 Brimonidine for system suitability 1.3 mg EPY0001658 Brimonidine tartrate 5 mg EPB1143000 Bromazepam 60 mg EPY0000645 Bromazepam for system suitability Controlled Substance 10 mg EPB1145000 Bromhexine hydrochloride 100 mg

    EPY0000200 Bromhexine impurity C N-(2-aminobenzyl)-N-methylcyclohexanamine

    15 mg

    EPB1150000 Bromocriptine mesilate 30 mg EPY0000677 Bromocriptine mesilate for system suitability 5 mg EPB1152000 Bromperidol 100 mg EPB1152050 Bromperidol decanoate 60 mg EPB1153000 Brompheniramine maleate 100 mg EPY0000468 Brotizolam 10 mg

    EPY0000470

    Brotizolam impurity B 2-bromo-4-(2-chlorophenyl)-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine (demethylbrotizolam)

    10 mg

    EPB1155000 Brucella melitensis Rev. 1 strain BRP 1 mL EPB1157300 Budesonide 110 mg EPY0001148 Budesonide for system suitability 10 mg EPB1156000 Bufexamac 100 mg EPY0001529 Buflomedil for peak identification 0.45 mg EPB1157400 Buflomedil hydrochloride 100 mg

    EPB1157410 Buflomedil impurity B 4-(pyrrolidin-1-yl)-1-(4-hydroxy-2,6-dimethoxyphenyl)butan-1-one

    20 mg

    EPB1158000 Bumetanide 150 mg

    EPY0000309 Bumetanide impurity A 3-nitro-4-phenoxy-5-sulphamoylbenzoic acid

    5 mg

    EPY0000310

    Bumetanide impurity B 3-amino-4-phenoxy-5-sulphamoylbenzoic acid

    5 mg

    EPB1160000 Bupivacaine hydrochloride 100 mg

    EPY0000088 Bupivacaine impurity B (2RS)-N-(2,6-dimethylphenyl)piperidine-2-carboxamide

    20 mg

    EPY0000089

    Bupivacaine impurity E 6-(butylamino)-N-(2,6-dimethylphenyl)hexanamide

    20 mg

    EPY0001575

    Bupivacaine impurity F 2,6-dimethylaniline

    70 mg

    EPY0001108 Buprenorphine 10 mg EPY0001122 Buprenorphine for system suitability Controlled Substance 10 mg EPY0001109 Buprenorphine hydrochloride 10 mg EPB1168000 Buserelin 2 mg EPY0000471 Buspirone for system suitability 2 mg EPY0000131 Buspirone hydrochloride 5 mg EPB1170000 Busulfan 50 mg EPY0001487 Butyl methacrylate 100 mg EPY0001304 Butyl methanesulfonate 30 µl

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  • European Pharmacopoeia

    22 Visit us at www.lgcstandards.com Edition 2014

    Code Product Unit

    EPB1217000 Butyl parahydroxybenzoate 100 mg

    EPY0001357 Butyl parahydroxybenzoate impurity E 2-methylpropyl 4-hydroxybenzoate (iso-butyl parahydroxybenzoate)

    15 mg

    EPB1212000 Butylhydroxyanisole 60 mg EPB1215000 Butylhydroxytoluene Plastic additive 07 50 mg EPY0000472 Cabergoline 100 mg EPC0100000 Caffeine 70 mg EPY0000787 Caffeine for system suitability 10 mg EPC0166000 Calcifediol 5 mg EPC0166001 Calcifediol - Reference Spectrum unit EPY0000499 Calcipotriol (anhydrous) - Reference Spectrum unit EPY0000473 Calcipotriol monohydrate 10 mg EPY0000474 Calcipotriol monohydrate - Reference Spectrum unit EPC0200000 Calcitonin (salmon) 2x1 mg EPY0000632 Calcitonin-Gly 0.4 mL EPC0225000 Calcitriol 10 mg EPC0226000 Calcitriol - Reference Spectrum unit EPC0249000 Calcium ascorbate - Reference Spectrum unit EPC0250000 Calcium folinate 130 mg EPC0299000 Calcium glucoheptonate 60 mg EPC0300000 Calcium gluconate 100 mg EPC0340000 Calcium levulinate dihydrate 250 mg EPC0350000 Calcium oxalate monohydrate 500 mg EPC0400000 Calcium pantothenate 60 mg EPC0405000 Camphor (racemic) 50 mg EPY0001388 Candesartan cilexetil 60 mg EPY0001387 Candesartan cilexetil for peak identification 10 mg EPY0001389 Candesartan cilexetil for system suitability 10 mg EPC0410000 Canrenone 50 mg EPY0001642 Capecitabine 150 mg

    EPY0001643

    Capecitabine impurity A 4-amino-1-(5-deoxy-ß-D-ribofuranosyl)-5-fluoropyrimidin-2(1H)-one (5'-deoxy-5-fluorocytidine)

    5 mg

    EPY0001644

    Capecitabine impurity B 1-(5-deoxy-ß-D-ribofuranosyl)-5-fluoropyrimidin-2,4(1H,3H)-dione (5'-deoxy-5-fluorocytidine)

    5 mg

    EPY0001645

    Capecitabine impurity D (2RS)-2-methylbutyl [1-(5-deoxy-ß-D-ribofuranosyl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl]carbamate

    10 mg

    EPC0426000 Caprylic acid 100 mg EPY0000671 Capsaicin 50 mg EPC0430000 Captopril 10 mg EPY0001182 Captopril for system suitability 20 mg

    EPY0001219 Captopril impurity B (2S) 1-[(2S)-3-bromo-2-methylpropanoyl]pyrrolidine-2-carboxylic acid

    10 mg

    EPY0001220

    Captopril impurity C (2RS)-2-methyl-3-sulphanylpropanoic acid

    10 mg

    EPY0001221

    Captopril impurity D (2RS)-3-bromo-2-methylpropanoic acid

    10 mg

    EPY0000435

    Captopril impurity E (2S)-1-isobutyryl-pyrrolidine-2-carboxylic acid

    10 mg

    EPY0001450

    Captopril impurity J (2S)-1-[(2S)-3-(acetylsulfanyl)-2-methylpropanoyl]pyrrolidine-2-carboxylic acid (acetylcaptopril)

    10 mg

    EPY0000113 Carbachol 50 mg EPC0450000 Carbamazepine 200 mg

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  • European Pharmacopoeia

    Edition 2014 Visit us at www.lgcstandards.com 23

    Code Product Unit

    EPY0000033

    Carbamazepine impurity A 10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide(10,11-dihydrocarbamazepine)

    10 mg

    EPC0451000 Carbasalate calcium - Reference Spectrum unit

    EPY0001161 Carbasalate impurity B 2-[[2-(acetyloxy)benzoyl]oxy]benzoic acid (acetylsalicylsalicylic acid)

    5 mg

    EPC0455000 Carbenicillin sodium 50 mg EPC0460000 Carbidopa 50 mg EPC0465000 Carbimazole 120 mg EPC0470000 Carbocisteine 60 mg EPC0499900 Carbon dioxide - Reference Spectrum unit EPC0550000 Carboplatin - Reference Spectrum unit EPY0000475 Carboprost trometamol 40 mg EPY0000536 Carboprost trometamol - Reference Spectrum unit EPY0000035 Carisoprodol 50 mg

    EPY0000036 Carisoprodol impurity A (2RS)-2-(hydroxymethyl)-2-methylpentyl(1-methylethyl)carbamate

    10 mg

    EPY0001214 Carmellose 10 mg EPC0580004 Carmustine - Reference Spectrum unit

    EPC0580010 Carmustine impurity A 1,3-bis(2-chloroethyl)urea

    20 mg

    EPY0000884 Carprofen for system suitability 5 mg EPY0000846 Carprofen for veterinary use 30 mg EPY0000193 Carteolol for system suitability 30 mg EPY0000192 Carteolol hydrochloride - Reference Spectrum unit EPY0001427 Carvedilol 50 mg EPY0000075 Carvedilol - Reference Spectrum unit EPY0001426 Carvedilol for system suitability 10 mg

    EPY0000103 Carvedilol impurity C (2RS)-1-[benzyl[2-(2-methoxyphenoxy)ethyl]amino]-3-(9H-carbazol-4-yloxy) propan-2-ol

    15 mg

    EPC0600000 Casein BRP 100 g EPC0630000 Cefaclor 450 mg EPC0650000 Cefadroxil 250mg EPC0675000 Cefalexin monohydrate 150 mg EPY0000505 Cefalotin for impurity B identification 10 mg EPC0682000 Cefalotin sodium 100 mg EPC0682300 Cefamandole nafate 125 mg EPY0000240 Cefapirin sodium 100 mg

    EPC0682410

    Cefatrizine impurity A 7-amino-(6R,7R)-3-[(2H-1,2,3-triazol-4-yl)sulfanyl]-methyl-8-oxo-5-thia-1-azabicyclo[4.2.O]oct-2-ene-2-carboxylic acid(7-ACA triazole)

    60 mg

    EPC0682400 Cefatrizine propylene glycol 150 mg EPC0682800 Cefazolin 150 mg EPY0000633 Cefepime dihydrochloride monohydrate 150 mg EPY0000634 Cefepime dihydrochloride monohydrate for system suitability 15 mg

    EPY0001336

    Cefepime impurity E (6R,7R)-7-amino-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

    10 mg

    EPC0684000 Cefixime 200 mg EPC0684750 Cefoperazone dihydrate 100 mg EPC0684800 Cefoperazone sodium - Reference Spectrum unit EPY0000420 Cefotaxime acid 80 mg EPY0000506 Cefotaxime for peak identification 10 mg EPC0685000 Cefotaxime sodium 30 mg EPC0688000 Cefoxitin sodium 100 mg

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  • European Pharmacopoeia

    24 Visit us at www.lgcstandards.com Edition 2014

    Code Product Unit

    EPY0001496 Cefoxitin sodium for peak identification 15 mg EPY0001305 Cefpodoxime proxetil 70 mg EPY0001318 Cefpodoxime proxetil for impurity H identification 10 mg EPY0001306 Cefpodoxime proxetil for peak identification 10 mg EPY0001371 Cefprozil 120 mg EPY0001367 Cefprozil for peak identification 10 mg

    EPY0001372 Cefprozil impurity A (2R)-2-amino-2-(4-hydroxyphenyl)acetic acid (p-hydroxyphenylglycine)

    20 mg

    EPY0001368 Cefprozil impurity mixture 10 mg EPC0690000 Cefradine 300 mg EPY0000568 Cefradine for peak identification 15 mg EPY0001174 Cefradine impurity mixture 0.04 mg EPC0690500 Ceftazidime 200 mg EPY0001111 Ceftazidime for peak identification 10 mg

    EPC0692000 Ceftriaxone impurity A E-isomer

    10 mg

    EPC0691000 Ceftriaxone sodium 100 mg EPC0694990 Cefuroxime axetil 60 mg EPC0695000 Cefuroxime sodium 150 mg EPY0001445 Celecoxib 200 mg

    EPY0001446 Celecoxib impurity A 4-[5-(3-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide

    10 mg

    EPY0001447

    Celecoxib impurity B 4-[3-(4-methylphenyl)-5-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide

    10 mg

    EPY0000239 Celiprolol for peak identification 20 mg EPY0000311 Celiprolol hydrochloride 10 mg

    EPY0000312 Celiprolol impurity I 1-acetyl-1-(4-ethoxyphenyl)-3,3-diethylurea

    0.02 mg

    EPY0000784 Cellulose acetate 40 mg EPY0001585 Cellulose acetate butyrate 60 mg EPY0001054 Cellulose acetate phthalate 10 mg EPC0700000 Cephaeline hydrochloride 15 mg EPC0980650 Cetirizine dihydrochloride 100 mg EPY0001197 Cetirizine for peak identification 1.01 mg

    EPC0980651 Cetirizine impurity A (RS)-1-[(4-chlorophenyl)phenylmethyl]piperazine

    10 mg

    EPC0984100 Cetostearyl isononanoate - Reference Spectrum unit EPC0990000 Cetyl alcohol 250 mg EPY0000073 Cetyl palmitate 15 60 mg EPY0000074 Cetyl palmitate 95 50 mg EPC1000000 Cetylpyridinium chloride 20 mg EPC1050000 Chenodeoxycholic acid 125 mg EPY0000104 Chitosan hydrochloride 30 mg EPC1100000 Chlorambucil 100 mg EPY0001298 Chlorambucil for system suitability 10 mg EPY0001299 Chlorambucil with impurity G 10 mg EPC1200000 Chloramphenicol 500 mg EPC1300000 Chloramphenicol dipalmitate 100 mg EPC1350000 Chloramphenicol disodium disuccinate 25 mg EPC1400000 Chloramphenicol palmitate isomer 100 mg EPC1425000 Chloramphenicol sodium succinate 1500 mg EPC1435000 Chlorcyclizine hydrochloride 100 mg EPC1450000 Chlordiazepoxide Controlled Substance 2x50 mg

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