IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 1PHARMACEUTICAL WORKS POLPHARMA S.A. Starogard Gdanski PL
03 2COHANCE LIFESCIENCES LIMITED Hyderabad IN
04 1UNIMARK REMEDIES LIMITED Mumbai IN
05 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
06 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
07 1ARAGEN LIFE SCIENCES LIMITED Hyderabad IN
08 1CIPLA LIMITED Mumbai IN
09 1CTX LIFESCIENCES PVT. LIMITED Surat IN
10 1IPCA Laboratories Limited Mumbai IN
11 1JUBILANT PHARMOVA LIMITED Nanjangud IN
12 1SEQUEL PHARMACHEM PRIVATE LTD. Nerul IN
13 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
14 1TAPI NL B.V. Amsterdam NL
15 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
16 1TORRENT PHARMACEUTICALS LIMITED Ahmedabad IN
17 1Unichem Laboratories Limited Mumbai IN
18 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
19 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
20 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
21 1Zhejiang Supor Pharmaceuticals Co., Ltd. Shaoxing CN
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : R1-CEP 2013-066 - Rev 01
Status : Valid
Issue Date : 2023-01-09
Type : Chemical
Substance Number : 1756
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Certificate Number : R1-CEP 2010-128 - Rev 02
Status : Valid
Issue Date : 2023-02-16
Type : Chemical
Substance Number : 1756
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : R0-CEP 2022-417 - Rev 00
Status : Valid
Issue Date : 2022-12-15
Type : Chemical
Substance Number : 1756
Certificate Number : R1-CEP 2009-278 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2016-02-26
Type : Chemical
Substance Number : 1756
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : R1-CEP 2008-261 - Rev 02
Status : Valid
Issue Date : 2022-12-15
Type : Chemical
Substance Number : 1756
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PharmaCompass offers a list of Lamotrigine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Lamotrigine manufacturer or Lamotrigine supplier for your needs.
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A Lamotrigine, British Pharmacopoeia (BP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lamotrigine, British Pharmacopoeia (BP) Reference Standard, including repackagers and relabelers. The FDA regulates Lamotrigine, British Pharmacopoeia (BP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lamotrigine, British Pharmacopoeia (BP) Reference Standard API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lamotrigine, British Pharmacopoeia (BP) Reference Standard supplier is an individual or a company that provides Lamotrigine, British Pharmacopoeia (BP) Reference Standard active pharmaceutical ingredient (API) or Lamotrigine, British Pharmacopoeia (BP) Reference Standard finished formulations upon request. The Lamotrigine, British Pharmacopoeia (BP) Reference Standard suppliers may include Lamotrigine, British Pharmacopoeia (BP) Reference Standard API manufacturers, exporters, distributors and traders.
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A Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP of the European Pharmacopoeia monograph is often referred to as a Lamotrigine, British Pharmacopoeia (BP) Reference Standard Certificate of Suitability (COS). The purpose of a Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Lamotrigine, British Pharmacopoeia (BP) Reference Standard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Lamotrigine, British Pharmacopoeia (BP) Reference Standard to their clients by showing that a Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP has been issued for it. The manufacturer submits a Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP holder for the record. Additionally, the data presented in the Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Lamotrigine, British Pharmacopoeia (BP) Reference Standard DMF.
A Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Lamotrigine, British Pharmacopoeia (BP) Reference Standard CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 20 companies offering Lamotrigine, British Pharmacopoeia (BP) Reference Standard
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