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01 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
02 1CIPLA LIMITED Mumbai IN
03 1GlaxoSmithKline Research & Development Limited Greenford GB
04 1HETERO LABS LIMITED Hyderabad IN
05 1SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
06 1ST PHARM CO., LTD. Siheung-Si KR
07 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
08 1Yuhan Chemical Inc. Ansan-Shi, Kyunggi-Do KR
09 1ZHEJIANG LANGHUA PHARMACEUTICAL CO., LTD. Linhai CN
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01 9Zidovudine
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01 2China
02 4India
03 2South Korea
04 1United Kingdom
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01 1Expired
02 4Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 3Withdrawn by Holder
Certificate Number : CEP 2005-063 - Rev 05
Status : Valid
Issue Date : 2023-11-28
Type : Chemical
Substance Number : 1059
Certificate Number : R1-CEP 2008-125 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2018-05-02
Type : Chemical
Substance Number : 1059
Certificate Number : R1-CEP 2001-321 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2008-03-06
Type : Chemical
Substance Number : 1059
Certificate Number : CEP 2008-333 - Rev 07
Status : Valid
Issue Date : 2025-05-23
Type : Chemical
Substance Number : 1059
Certificate Number : R0-CEP 2021-015 - Rev 00
Status : Valid
Issue Date : 2022-07-13
Type : Chemical
Substance Number : 1059
Certificate Number : R1-CEP 1998-117 - Rev 03
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2012-01-23
Type : Chemical
Substance Number : 1059
Certificate Number : CEP 2007-318 - Rev 06
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 1059
Certificate Number : R0-CEP 2004-035 - Rev 00
Status : Expired
Issue Date : 2005-11-14
Type : Chemical
Substance Number : 1059
Certificate Number : R1-CEP 2012-341 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2021-01-18
Type : Chemical
Substance Number : 1059
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PharmaCompass offers a list of Zidovudine 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 Zidovudine manufacturer or Zidovudine supplier for your needs.
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A Tox21_300578 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300578, including repackagers and relabelers. The FDA regulates Tox21_300578 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300578 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 Tox21_300578 supplier is an individual or a company that provides Tox21_300578 active pharmaceutical ingredient (API) or Tox21_300578 finished formulations upon request. The Tox21_300578 suppliers may include Tox21_300578 API manufacturers, exporters, distributors and traders.
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A Tox21_300578 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_300578 Certificate of Suitability (COS). The purpose of a Tox21_300578 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_300578 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_300578 to their clients by showing that a Tox21_300578 CEP has been issued for it. The manufacturer submits a Tox21_300578 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_300578 CEP holder for the record. Additionally, the data presented in the Tox21_300578 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_300578 DMF.
A Tox21_300578 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_300578 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 9 companies offering Tox21_300578
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