01 1IPCA Laboratories Limited Mumbai IN
02 1UNICHEM LABORATORIES LIMITED Mumbai IN
01 2Bendroflumethiazide
01 2India
01 2Valid
Certificate Number : R1-CEP 2007-142 - Rev 03
Status : Valid
Issue Date : 2018-04-23
Type : Chemical
Substance Number : 370
Certificate Number : CEP 2002-102 - Rev 02
Status : Valid
Issue Date : 2024-11-05
Type : Chemical
Substance Number : 370
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PharmaCompass offers a list of Bendroflumethiazide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Bendroflumethiazide manufacturer or Bendroflumethiazide supplier for your needs.
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A Flumesil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumesil, including repackagers and relabelers. The FDA regulates Flumesil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumesil 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 Flumesil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flumesil supplier is an individual or a company that provides Flumesil active pharmaceutical ingredient (API) or Flumesil finished formulations upon request. The Flumesil suppliers may include Flumesil API manufacturers, exporters, distributors and traders.
click here to find a list of Flumesil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Flumesil CEP of the European Pharmacopoeia monograph is often referred to as a Flumesil Certificate of Suitability (COS). The purpose of a Flumesil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flumesil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flumesil to their clients by showing that a Flumesil CEP has been issued for it. The manufacturer submits a Flumesil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flumesil CEP holder for the record. Additionally, the data presented in the Flumesil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flumesil DMF.
A Flumesil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flumesil 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 Flumesil suppliers with CEP (COS) on PharmaCompass.
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