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Status : Withdrawn by Holder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Status : Withdrawn by Holder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 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 : 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Status : Withdrawn by EDQM Failure to CEP pro...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 : 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Status : Withdrawn by Holder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Status : Withdrawn by Holder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
57
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zidovudine manufacturer or Zidovudine supplier.
PharmaCompass also assists you with knowing the Zidovudine API Price utilized in the formulation of products. Zidovudine API Price is not always fixed or binding as the Zidovudine Price is obtained through a variety of data sources. The Zidovudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ZVD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZVD, including repackagers and relabelers. The FDA regulates ZVD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZVD 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 ZVD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ZVD supplier is an individual or a company that provides ZVD active pharmaceutical ingredient (API) or ZVD finished formulations upon request. The ZVD suppliers may include ZVD API manufacturers, exporters, distributors and traders.
click here to find a list of ZVD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ZVD CEP of the European Pharmacopoeia monograph is often referred to as a ZVD Certificate of Suitability (COS). The purpose of a ZVD CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ZVD EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ZVD to their clients by showing that a ZVD CEP has been issued for it. The manufacturer submits a ZVD CEP (COS) as part of the market authorization procedure, and it takes on the role of a ZVD CEP holder for the record. Additionally, the data presented in the ZVD CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ZVD DMF.
A ZVD CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ZVD 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 ZVD suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering ZVD
Get in contact with the supplier of your choice:
