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Status : Withdrawn by Holder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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Stavudine manufacturer or Stavudine supplier.
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 Sazi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sazi, including repackagers and relabelers. The FDA regulates Sazi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sazi 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 Sazi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sazi supplier is an individual or a company that provides Sazi active pharmaceutical ingredient (API) or Sazi finished formulations upon request. The Sazi suppliers may include Sazi API manufacturers, exporters, distributors and traders.
click here to find a list of Sazi suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sazi CEP of the European Pharmacopoeia monograph is often referred to as a Sazi Certificate of Suitability (COS). The purpose of a Sazi CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sazi EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sazi to their clients by showing that a Sazi CEP has been issued for it. The manufacturer submits a Sazi CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sazi CEP holder for the record. Additionally, the data presented in the Sazi CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sazi DMF.
A Sazi CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sazi 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 Sazi suppliers with CEP (COS) on PharmaCompass.
