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Status : Withdrawn by Holder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
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 1999-137 - Rev 08
Status : Valid
Issue Date : 2021-08-20
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 Diumide-K manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diumide-K, including repackagers and relabelers. The FDA regulates Diumide-K manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diumide-K 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 Diumide-K manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diumide-K supplier is an individual or a company that provides Diumide-K active pharmaceutical ingredient (API) or Diumide-K finished formulations upon request. The Diumide-K suppliers may include Diumide-K API manufacturers, exporters, distributors and traders.
click here to find a list of Diumide-K suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diumide-K CEP of the European Pharmacopoeia monograph is often referred to as a Diumide-K Certificate of Suitability (COS). The purpose of a Diumide-K CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Diumide-K EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Diumide-K to their clients by showing that a Diumide-K CEP has been issued for it. The manufacturer submits a Diumide-K CEP (COS) as part of the market authorization procedure, and it takes on the role of a Diumide-K CEP holder for the record. Additionally, the data presented in the Diumide-K CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Diumide-K DMF.
A Diumide-K CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Diumide-K 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 Diumide-K suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Diumide-K
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