01 2R L FINE CHEM PVT. LTD. Gowribidanur IN
02 1SIGMA-ALDRICH IRELAND LTD Arklow IE
03 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
01 3Doxylamine hydrogen succinate
02 1Doxylamine hydrogen succinate, Grade II
01 2India
02 1Spain
03 1U.S.A
01 4Valid
Certificate Number : CEP 2018-041 - Rev 03
Status : Valid
Issue Date : 2025-03-24
Type : Chemical
Substance Number : 1589
Doxylamine Hydrogen Succinate, Grade II
Certificate Number : CEP 2021-283 - Rev 02
Status : Valid
Issue Date : 2025-03-26
Type : Chemical
Substance Number : 1589
Certificate Number : CEP 2004-167 - Rev 02
Status : Valid
Issue Date : 2025-01-29
Type : Chemical
Substance Number : 1589
Certificate Number : R1-CEP 2004-089 - Rev 06
Status : Valid
Issue Date : 2020-10-21
Type : Chemical
Substance Number : 1589
15
PharmaCompass offers a list of Doxylamine Succinate 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 Doxylamine Succinate manufacturer or Doxylamine Succinate supplier for your needs.
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A Unisom manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Unisom, including repackagers and relabelers. The FDA regulates Unisom manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Unisom 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 Unisom supplier is an individual or a company that provides Unisom active pharmaceutical ingredient (API) or Unisom finished formulations upon request. The Unisom suppliers may include Unisom API manufacturers, exporters, distributors and traders.
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A Unisom CEP of the European Pharmacopoeia monograph is often referred to as a Unisom Certificate of Suitability (COS). The purpose of a Unisom CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Unisom EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Unisom to their clients by showing that a Unisom CEP has been issued for it. The manufacturer submits a Unisom CEP (COS) as part of the market authorization procedure, and it takes on the role of a Unisom CEP holder for the record. Additionally, the data presented in the Unisom CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Unisom DMF.
A Unisom CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Unisom 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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