USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
01 1USV PRIVATE LIMITED Mumbai IN
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1Calao s.r.l. Milano IT
04 1ELIXIR PHARMA Ahmedabad IN
05 1F Hoffmann-La Roche Ltd. Basel CH
06 1LUSOCHIMICA S.P.A. Pisa IT
07 1Orgapharm Pithiviers FR
08 1SRI KRISHNA PHARMACEUTICALS LIMITED Hyderabad IN
09 1ZENTIVA K.S. Praha 10 CZ
01 6Glibenclamide
02 1Glibenclamide, Micronised
03 1Glibenclamide, Milled
04 1Glibenclamide, Non-micronised, micronised
01 1Czech Republic
02 1France
03 4India
04 1Italy
05 2U.S.A
01 7Valid
02 2Withdrawn by Holder
Glibenclamide, Non-micronised, Micronised
Certificate Number : CEP 2000-090 - Rev 05
Status : Valid
Issue Date : 2024-04-19
Type : Chemical
Substance Number : 718
Certificate Number : CEP 2004-192 - Rev 06
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 718
Certificate Number : R1-CEP 2006-134 - Rev 02
Status : Valid
Issue Date : 2013-07-19
Type : Chemical
Substance Number : 718
Certificate Number : R0-CEP 2001-361 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2006-10-05
Type : Chemical
Substance Number : 718
Certificate Number : R1-CEP 2012-042 - Rev 00
Status : Valid
Issue Date : 2019-09-13
Type : Chemical
Substance Number : 718
Certificate Number : R1-CEP 1999-003 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2009-11-19
Type : Chemical
Substance Number : 718
Certificate Number : R1-CEP 2005-195 - Rev 00
Status : Valid
Issue Date : 2014-05-22
Type : Chemical
Substance Number : 718
Certificate Number : CEP 2000-289 - Rev 10
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 718
Certificate Number : R1-CEP 2003-223 - Rev 07
Status : Valid
Issue Date : 2022-02-08
Type : Chemical
Substance Number : 718
A Glibenclamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glibenclamide, including repackagers and relabelers. The FDA regulates Glibenclamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glibenclamide 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 Glibenclamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glibenclamide supplier is an individual or a company that provides Glibenclamide active pharmaceutical ingredient (API) or Glibenclamide finished formulations upon request. The Glibenclamide suppliers may include Glibenclamide API manufacturers, exporters, distributors and traders.
click here to find a list of Glibenclamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glibenclamide CEP of the European Pharmacopoeia monograph is often referred to as a Glibenclamide Certificate of Suitability (COS). The purpose of a Glibenclamide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Glibenclamide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Glibenclamide to their clients by showing that a Glibenclamide CEP has been issued for it. The manufacturer submits a Glibenclamide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Glibenclamide CEP holder for the record. Additionally, the data presented in the Glibenclamide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Glibenclamide DMF.
A Glibenclamide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Glibenclamide 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 Glibenclamide suppliers with CEP (COS) on PharmaCompass.
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