01 1AARTI DRUGS LIMITED Mumbai IN
02 1Erregierre S.p.A. San Paolo D'Argon IT
03 1FLAMMA S.P.A. Chignolo d'Isola IT
04 1HAS HEALTHCARE ADVANCED SYNTHESIS SA Biasca CH
05 1MANGALAM DRUGS & ORGANICS LTD. Mumbai IN
06 1Recordati S.p.A. Milano IT
01 5Nimesulide
02 1Nimesulide, Micronised
01 2India
02 3Italy
03 1Switzerland
01 1Expired
02 4Valid
03 1Withdrawn by Holder
Certificate Number : R1-CEP 2002-046 - Rev 06
Status : Valid
Issue Date : 2019-05-03
Type : Chemical
Substance Number : 1548
Certificate Number : R1-CEP 2005-201 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2014-04-23
Type : Chemical
Substance Number : 1548
Certificate Number : R1-CEP 2004-117 - Rev 01
Status : Valid
Issue Date : 2015-11-13
Type : Chemical
Substance Number : 1548
Certificate Number : R1-CEP 2010-377 - Rev 02
Status : Valid
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 1548
Certificate Number : R1-CEP 2011-310 - Rev 01
Status : Valid
Issue Date : 2023-03-13
Type : Chemical
Substance Number : 1548
Certificate Number : R0-CEP 2002-109 - Rev 01
Status : Expired
Issue Date : 2004-11-30
Type : Chemical
Substance Number : 1548
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PharmaCompass offers a list of Nimesulide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Nimesulide manufacturer or Nimesulide supplier for your needs.
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PharmaCompass also assists you with knowing the Nimesulide API Price utilized in the formulation of products. Nimesulide API Price is not always fixed or binding as the Nimesulide Price is obtained through a variety of data sources. The Nimesulide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C13H12N2O5S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C13H12N2O5S, including repackagers and relabelers. The FDA regulates C13H12N2O5S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C13H12N2O5S API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A C13H12N2O5S supplier is an individual or a company that provides C13H12N2O5S active pharmaceutical ingredient (API) or C13H12N2O5S finished formulations upon request. The C13H12N2O5S suppliers may include C13H12N2O5S API manufacturers, exporters, distributors and traders.
click here to find a list of C13H12N2O5S suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A C13H12N2O5S CEP of the European Pharmacopoeia monograph is often referred to as a C13H12N2O5S Certificate of Suitability (COS). The purpose of a C13H12N2O5S CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C13H12N2O5S EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C13H12N2O5S to their clients by showing that a C13H12N2O5S CEP has been issued for it. The manufacturer submits a C13H12N2O5S CEP (COS) as part of the market authorization procedure, and it takes on the role of a C13H12N2O5S CEP holder for the record. Additionally, the data presented in the C13H12N2O5S CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C13H12N2O5S DMF.
A C13H12N2O5S CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C13H12N2O5S 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 C13H12N2O5S suppliers with CEP (COS) on PharmaCompass.
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