EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI GERMANY GmbH Frankfurt am Main DE
02 1CURIA INDIA PRIVATE LIMITED Hyderabad IN
03 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
04 1IPCA Laboratories Limited Mumbai IN
05 1MANGALAM DRUGS & ORGANICS LTD. Mumbai IN
06 1OLON S.P.A. Rodano IT
07 2SRI KRISHNA PHARMACEUTICALS LIMITED Hyderabad IN
08 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
01 8Furosemide
02 1Furosemide, Alternative process
01 1France
02 5India
03 1Israel
04 2Italy
01 8Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2005-274 - Rev 03
Status : Valid
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 391
Certificate Number : R1-CEP 1999-069 - Rev 09
Status : Valid
Issue Date : 2021-08-09
Type : Chemical
Substance Number : 391
Certificate Number : R1-CEP 2004-005 - Rev 03
Status : Valid
Issue Date : 2014-02-24
Type : Chemical
Substance Number : 391
Certificate Number : R1-CEP 1998-020 - Rev 07
Status : Valid
Issue Date : 2019-10-30
Type : Chemical
Substance Number : 391
Certificate Number : R0-CEP 2019-063 - Rev 01
Status : Valid
Issue Date : 2023-03-02
Type : Chemical
Substance Number : 391
Certificate Number : R2-CEP 1992-012 - Rev 05
Status : Withdrawn by Holder
Issue Date : 2016-09-09
Type : Chemical
Substance Number : 391
Certificate Number : R1-CEP 1999-137 - Rev 08
Status : Valid
Issue Date : 2021-08-20
Type : Chemical
Substance Number : 391
Furosemide, Alternative Process
Certificate Number : R1-CEP 2013-273 - Rev 00
Status : Valid
Issue Date : 2018-12-04
Type : Chemical
Substance Number : 391
Certificate Number : R1-CEP 1997-019 - Rev 09
Status : Valid
Issue Date : 2021-12-20
Type : Chemical
Substance Number : 391
A Furosemide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Furosemide, including repackagers and relabelers. The FDA regulates Furosemide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Furosemide 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 Furosemide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Furosemide supplier is an individual or a company that provides Furosemide active pharmaceutical ingredient (API) or Furosemide finished formulations upon request. The Furosemide suppliers may include Furosemide API manufacturers, exporters, distributors and traders.
click here to find a list of Furosemide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Furosemide CEP of the European Pharmacopoeia monograph is often referred to as a Furosemide Certificate of Suitability (COS). The purpose of a Furosemide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Furosemide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Furosemide to their clients by showing that a Furosemide CEP has been issued for it. The manufacturer submits a Furosemide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Furosemide CEP holder for the record. Additionally, the data presented in the Furosemide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Furosemide DMF.
A Furosemide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Furosemide 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 Furosemide suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Furosemide
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