01 APITORIA PHARMA PRIVATE LIMITED Hyderabad IN (1)
02 CIPLA LIMITED Mumbai IN (1)
03 GlaxoSmithKline Research & Development Limited Greenford GB (1)
04 HETERO LABS LIMITED Hyderabad IN (1)
05 MATRIX LABORATORIES (XIAMEN) LTD. Xiamen CN (1)
06 MYLAN LABORATORIES LIMITED Hyderabad IN (1)
07 Medichem, S.A. Celrà ES (1)
08 SHANGHAI DESANO CHEMICAL PHARMACEUTICAL CO., LTD. Laogang Town CN (1)
09 ST PHARM CO., LTD. Siheung-Si KR (1)
10 Yuhan Chemical Inc. Ansan-Shi, Kyunggi-Do KR (1)
11 ZHEJIANG LANGHUA PHARMACEUTICAL CO., LTD. Linhai CN (1)
01 Zidovudine (11)
01 China (3)
02 India (3)
03 South Korea (2)
04 Spain (1)
05 U.S.A (1)
06 United Kingdom (1)
01 Expired (1)
02 Valid (5)
03 Withdrawn by EDQM Failure to CEP procedure (2)
04 Withdrawn by Holder (3)
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 Zidovudine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zidovudine, including repackagers and relabelers. The FDA regulates Zidovudine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zidovudine 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 Zidovudine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zidovudine supplier is an individual or a company that provides Zidovudine active pharmaceutical ingredient (API) or Zidovudine finished formulations upon request. The Zidovudine suppliers may include Zidovudine API manufacturers, exporters, distributors and traders.
click here to find a list of Zidovudine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zidovudine CEP of the European Pharmacopoeia monograph is often referred to as a Zidovudine Certificate of Suitability (COS). The purpose of a Zidovudine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zidovudine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zidovudine to their clients by showing that a Zidovudine CEP has been issued for it. The manufacturer submits a Zidovudine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zidovudine CEP holder for the record. Additionally, the data presented in the Zidovudine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zidovudine DMF.
A Zidovudine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zidovudine 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 Zidovudine suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Zidovudine
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