01 1HY-GRO CHEMICALS PHARMTEK PRIVATE LIMITED Secunderabad IN
02 1SIEGFRIED LTD Zofingen CH
03 1Wockhardt Limited Mumbai IN
01 3Dextropropoxyphene hydrochloride
01 2India
02 1Switzerland
01 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Status : Withdrawn by Holder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Status : Withdrawn by Holder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Status : Withdrawn by Holder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
A Dextropropoxyphene HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextropropoxyphene HCl, including repackagers and relabelers. The FDA regulates Dextropropoxyphene HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextropropoxyphene HCl 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 Dextropropoxyphene HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextropropoxyphene HCl supplier is an individual or a company that provides Dextropropoxyphene HCl active pharmaceutical ingredient (API) or Dextropropoxyphene HCl finished formulations upon request. The Dextropropoxyphene HCl suppliers may include Dextropropoxyphene HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Dextropropoxyphene HCl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dextropropoxyphene HCl CEP of the European Pharmacopoeia monograph is often referred to as a Dextropropoxyphene HCl Certificate of Suitability (COS). The purpose of a Dextropropoxyphene HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dextropropoxyphene HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dextropropoxyphene HCl to their clients by showing that a Dextropropoxyphene HCl CEP has been issued for it. The manufacturer submits a Dextropropoxyphene HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dextropropoxyphene HCl CEP holder for the record. Additionally, the data presented in the Dextropropoxyphene HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dextropropoxyphene HCl DMF.
A Dextropropoxyphene HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dextropropoxyphene HCl 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 Dextropropoxyphene HCl suppliers with CEP (COS) on PharmaCompass.
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