01 1RAY CHEMICALS PRIVATE LIMITED Bangalore IN
02 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
01 2Dosulepin hydrochloride
01 2India
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R0-CEP 2010-009 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2012-11-26
Type : Chemical
Substance Number : 1314
Certificate Number : CEP 2003-157 - Rev 06
Status : Valid
Issue Date : 2025-07-25
Type : Chemical
Substance Number : 1314
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PharmaCompass offers a list of Dosulepin HCl 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 Dosulepin HCl manufacturer or Dosulepin HCl supplier for your needs.
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PharmaCompass also assists you with knowing the Dosulepin HCl API Price utilized in the formulation of products. Dosulepin HCl API Price is not always fixed or binding as the Dosulepin HCl Price is obtained through a variety of data sources. The Dosulepin HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Prothiaden hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prothiaden hydrochloride, including repackagers and relabelers. The FDA regulates Prothiaden hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prothiaden hydrochloride 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 Prothiaden hydrochloride supplier is an individual or a company that provides Prothiaden hydrochloride active pharmaceutical ingredient (API) or Prothiaden hydrochloride finished formulations upon request. The Prothiaden hydrochloride suppliers may include Prothiaden hydrochloride API manufacturers, exporters, distributors and traders.
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A Prothiaden hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Prothiaden hydrochloride Certificate of Suitability (COS). The purpose of a Prothiaden hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prothiaden hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prothiaden hydrochloride to their clients by showing that a Prothiaden hydrochloride CEP has been issued for it. The manufacturer submits a Prothiaden hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prothiaden hydrochloride CEP holder for the record. Additionally, the data presented in the Prothiaden hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prothiaden hydrochloride DMF.
A Prothiaden hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prothiaden hydrochloride 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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