01 1HETERO LABS LIMITED Hyderabad IN
01 1Stavudine
01 1India
01 1Withdrawn by Holder
Certificate Number : R1-CEP 2008-162 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2017-08-10
Type : Chemical
Substance Number : 2130
91
PharmaCompass offers a list of Stavudine 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 Stavudine manufacturer or Stavudine supplier for your needs.
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PharmaCompass also assists you with knowing the Stavudine API Price utilized in the formulation of products. Stavudine API Price is not always fixed or binding as the Stavudine Price is obtained through a variety of data sources. The Stavudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C07312 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07312, including repackagers and relabelers. The FDA regulates C07312 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07312 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 C07312 supplier is an individual or a company that provides C07312 active pharmaceutical ingredient (API) or C07312 finished formulations upon request. The C07312 suppliers may include C07312 API manufacturers, exporters, distributors and traders.
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A C07312 CEP of the European Pharmacopoeia monograph is often referred to as a C07312 Certificate of Suitability (COS). The purpose of a C07312 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C07312 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C07312 to their clients by showing that a C07312 CEP has been issued for it. The manufacturer submits a C07312 CEP (COS) as part of the market authorization procedure, and it takes on the role of a C07312 CEP holder for the record. Additionally, the data presented in the C07312 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C07312 DMF.
A C07312 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C07312 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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