Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LIMITED Mumbai IN
01 1Pheniramine maleate
01 1India
01 1Valid
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 2015-030 - Rev 01
Status : Valid
Issue Date : 2025-04-02
Type : Chemical
Substance Number : 1357
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PharmaCompass offers a list of Pheniramine Maleate 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 Pheniramine Maleate manufacturer or Pheniramine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Pheniramine Maleate API Price utilized in the formulation of products. Pheniramine Maleate API Price is not always fixed or binding as the Pheniramine Maleate Price is obtained through a variety of data sources. The Pheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trimetose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimetose, including repackagers and relabelers. The FDA regulates Trimetose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimetose 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 Trimetose supplier is an individual or a company that provides Trimetose active pharmaceutical ingredient (API) or Trimetose finished formulations upon request. The Trimetose suppliers may include Trimetose API manufacturers, exporters, distributors and traders.
click here to find a list of Trimetose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trimetose CEP of the European Pharmacopoeia monograph is often referred to as a Trimetose Certificate of Suitability (COS). The purpose of a Trimetose CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Trimetose EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Trimetose to their clients by showing that a Trimetose CEP has been issued for it. The manufacturer submits a Trimetose CEP (COS) as part of the market authorization procedure, and it takes on the role of a Trimetose CEP holder for the record. Additionally, the data presented in the Trimetose CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Trimetose DMF.
A Trimetose CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Trimetose 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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