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
Doxylamine Hydrogen Succinate, Grade II
Certificate Number : CEP 2021-283 - Rev 01
Status : Valid
Issue Date : 2024-02-08
Type : Chemical
Substance Number : 1589
Certificate Number : CEP 2018-041 - Rev 02
Status : Valid
Issue Date : 2024-03-01
Type : Chemical
Substance Number : 1589
Certificate Number : R1-CEP 2004-167 - Rev 01
Status : Valid
Issue Date : 2013-10-22
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
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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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PharmaCompass also assists you with knowing the Doxylamine Succinate API Price utilized in the formulation of products. Doxylamine Succinate API Price is not always fixed or binding as the Doxylamine Succinate Price is obtained through a variety of data sources. The Doxylamine Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Doxylamine Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxylamine Succinate, including repackagers and relabelers. The FDA regulates Doxylamine Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxylamine Succinate 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 Doxylamine Succinate supplier is an individual or a company that provides Doxylamine Succinate active pharmaceutical ingredient (API) or Doxylamine Succinate finished formulations upon request. The Doxylamine Succinate suppliers may include Doxylamine Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Doxylamine Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Doxylamine Succinate CEP of the European Pharmacopoeia monograph is often referred to as a Doxylamine Succinate Certificate of Suitability (COS). The purpose of a Doxylamine Succinate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Doxylamine Succinate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Doxylamine Succinate to their clients by showing that a Doxylamine Succinate CEP has been issued for it. The manufacturer submits a Doxylamine Succinate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Doxylamine Succinate CEP holder for the record. Additionally, the data presented in the Doxylamine Succinate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Doxylamine Succinate DMF.
A Doxylamine Succinate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Doxylamine Succinate 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 Doxylamine Succinate suppliers with CEP (COS) on PharmaCompass.
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