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
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PharmaCompass offers a list of Chlorpheniramine 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 Chlorpheniramine manufacturer or Chlorpheniramine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorpheniramine manufacturer or Chlorpheniramine supplier.
PharmaCompass also assists you with knowing the Chlorpheniramine API Price utilized in the formulation of products. Chlorpheniramine API Price is not always fixed or binding as the Chlorpheniramine Price is obtained through a variety of data sources. The Chlorpheniramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Clorfeniramina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clorfeniramina, including repackagers and relabelers. The FDA regulates Clorfeniramina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clorfeniramina 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 Clorfeniramina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clorfeniramina supplier is an individual or a company that provides Clorfeniramina active pharmaceutical ingredient (API) or Clorfeniramina finished formulations upon request. The Clorfeniramina suppliers may include Clorfeniramina API manufacturers, exporters, distributors and traders.
click here to find a list of Clorfeniramina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clorfeniramina CEP of the European Pharmacopoeia monograph is often referred to as a Clorfeniramina Certificate of Suitability (COS). The purpose of a Clorfeniramina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Clorfeniramina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Clorfeniramina to their clients by showing that a Clorfeniramina CEP has been issued for it. The manufacturer submits a Clorfeniramina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Clorfeniramina CEP holder for the record. Additionally, the data presented in the Clorfeniramina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Clorfeniramina DMF.
A Clorfeniramina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Clorfeniramina 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 Clorfeniramina suppliers with CEP (COS) on PharmaCompass.
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