01 1DIPHARMA FRANCIS S.R.L. Baranzate IT
02 1HY-GRO CHEMICALS PHARMTEK PRIVATE LIMITED Secunderabad IN
03 1SIEGFRIED LTD Zofingen CH
04 1Wockhardt Limited Mumbai IN
01 4Dextropropoxyphene hydrochloride
01 2India
02 1Italy
03 1Switzerland
01 1Expired
02 3Withdrawn by Holder
Dextropropoxyphene Hydrochloride
Certificate Number : R1-CEP 2002-161 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-03-09
Type : Chemical
Substance Number : 713
Dextropropoxyphene Hydrochloride
Certificate Number : R1-CEP 1996-068 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2007-05-21
Type : Chemical
Substance Number : 713
Dextropropoxyphene Hydrochloride
Certificate Number : R1-CEP 1998-096 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2010-07-12
Type : Chemical
Substance Number : 713
Dextropropoxyphene Hydrochloride
Certificate Number : R0-CEP 2001-396 - Rev 01
Status : Expired
Issue Date : 2005-11-03
Type : Chemical
Substance Number : 713
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PharmaCompass offers a list of Dextropropoxyphene 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 Dextropropoxyphene HCl manufacturer or Dextropropoxyphene HCl supplier for your needs.
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A Deprancol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deprancol, including repackagers and relabelers. The FDA regulates Deprancol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deprancol 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 Deprancol supplier is an individual or a company that provides Deprancol active pharmaceutical ingredient (API) or Deprancol finished formulations upon request. The Deprancol suppliers may include Deprancol API manufacturers, exporters, distributors and traders.
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A Deprancol CEP of the European Pharmacopoeia monograph is often referred to as a Deprancol Certificate of Suitability (COS). The purpose of a Deprancol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Deprancol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Deprancol to their clients by showing that a Deprancol CEP has been issued for it. The manufacturer submits a Deprancol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Deprancol CEP holder for the record. Additionally, the data presented in the Deprancol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Deprancol DMF.
A Deprancol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Deprancol 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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