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 1MATRIX LABORATORIES (XIAMEN) LTD. Xiamen CN
06 1Medichem, S.A. Celrà ES
07 1SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN
08 1ST PHARM CO., LTD. Siheung-Si KR
09 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
10 1Yuhan Chemical Inc. Ansan-Shi, Kyunggi-Do KR
11 1ZHEJIANG LANGHUA PHARMACEUTICAL CO., LTD. Linhai CN
01 11Zidovudine
01 3China
02 4India
03 2South Korea
04 1Spain
05 1United Kingdom
01 1Expired
02 4Valid
03 2Withdrawn by EDQM Failure to CEP procedure
04 4Withdrawn 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Status : Withdrawn by Holder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Status : Withdrawn by Holder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 06
Status : Valid
Issue Date : 2024-04-10
Type : Chemical
Substance Number : 1059
Certificate Number : R0-CEP 2003-276 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2009-08-28
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 : CEP 2007-318 - Rev 06
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 1059
Certificate Number : R1-CEP 1997-033 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2009-02-25
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Status : Withdrawn by Holder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
A AZT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AZT, including repackagers and relabelers. The FDA regulates AZT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AZT API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of AZT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AZT supplier is an individual or a company that provides AZT active pharmaceutical ingredient (API) or AZT finished formulations upon request. The AZT suppliers may include AZT API manufacturers, exporters, distributors and traders.
click here to find a list of AZT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AZT CEP of the European Pharmacopoeia monograph is often referred to as a AZT Certificate of Suitability (COS). The purpose of a AZT CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AZT EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AZT to their clients by showing that a AZT CEP has been issued for it. The manufacturer submits a AZT CEP (COS) as part of the market authorization procedure, and it takes on the role of a AZT CEP holder for the record. Additionally, the data presented in the AZT CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AZT DMF.
A AZT CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AZT CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of AZT suppliers with CEP (COS) on PharmaCompass.
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