Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1SUPRIYA LIFESCIENCE LTD. 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 : R1-CEP 2015-030 - Rev 00
Status : Valid
Issue Date : 2022-03-18
Type : Chemical
Substance Number : 1357
A Pheniramine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pheniramine, including repackagers and relabelers. The FDA regulates Pheniramine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pheniramine 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 Pheniramine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pheniramine supplier is an individual or a company that provides Pheniramine active pharmaceutical ingredient (API) or Pheniramine finished formulations upon request. The Pheniramine suppliers may include Pheniramine API manufacturers, exporters, distributors and traders.
click here to find a list of Pheniramine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pheniramine CEP of the European Pharmacopoeia monograph is often referred to as a Pheniramine Certificate of Suitability (COS). The purpose of a Pheniramine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Pheniramine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Pheniramine to their clients by showing that a Pheniramine CEP has been issued for it. The manufacturer submits a Pheniramine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Pheniramine CEP holder for the record. Additionally, the data presented in the Pheniramine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Pheniramine DMF.
A Pheniramine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Pheniramine 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 Pheniramine suppliers with CEP (COS) on PharmaCompass.
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