Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
02 1Auro Laboratories Limited Mumbai IN
03 1Kongo Chemical Co., Ltd Toyama City JP
01 3Chlorphenamine maleate
01 2India
02 1Japan
01 3Valid
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : CEP 2008-154 - Rev 03
Status : Valid
Issue Date : 2024-01-19
Type : Chemical
Substance Number : 386
Certificate Number : R1-CEP 2012-018 - Rev 00
Status : Valid
Issue Date : 2021-12-03
Type : Chemical
Substance Number : 386
Certificate Number : R1-CEP 2006-151 - Rev 01
Status : Valid
Issue Date : 2021-03-17
Type : Chemical
Substance Number : 386
A Chlorpheniramine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpheniramine, including repackagers and relabelers. The FDA regulates Chlorpheniramine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpheniramine 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 Chlorpheniramine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorpheniramine supplier is an individual or a company that provides Chlorpheniramine active pharmaceutical ingredient (API) or Chlorpheniramine finished formulations upon request. The Chlorpheniramine suppliers may include Chlorpheniramine API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorpheniramine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorpheniramine CEP of the European Pharmacopoeia monograph is often referred to as a Chlorpheniramine Certificate of Suitability (COS). The purpose of a Chlorpheniramine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Chlorpheniramine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Chlorpheniramine to their clients by showing that a Chlorpheniramine CEP has been issued for it. The manufacturer submits a Chlorpheniramine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Chlorpheniramine CEP holder for the record. Additionally, the data presented in the Chlorpheniramine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Chlorpheniramine DMF.
A Chlorpheniramine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Chlorpheniramine 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 Chlorpheniramine suppliers with CEP (COS) on PharmaCompass.
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