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Status : Withdrawn by Holder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
67
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 Zerit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zerit, including repackagers and relabelers. The FDA regulates Zerit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zerit 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 Zerit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zerit supplier is an individual or a company that provides Zerit active pharmaceutical ingredient (API) or Zerit finished formulations upon request. The Zerit suppliers may include Zerit API manufacturers, exporters, distributors and traders.
click here to find a list of Zerit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zerit CEP of the European Pharmacopoeia monograph is often referred to as a Zerit Certificate of Suitability (COS). The purpose of a Zerit CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zerit EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zerit to their clients by showing that a Zerit CEP has been issued for it. The manufacturer submits a Zerit CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zerit CEP holder for the record. Additionally, the data presented in the Zerit CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zerit DMF.
A Zerit CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zerit 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 Zerit suppliers with CEP (COS) on PharmaCompass.
