01 1Aarti Drugs
02 1Procos
03 1Vital Laboratories Private Limited
01 3NIMESULIDE
01 2India
02 1Italy
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20813
Submission : 2007-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15566
Submission : 2001-07-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25302
Submission : 2011-08-16
Status : Inactive
Type : II
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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.
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A C13H12N2O5S DMF (Drug Master File) is a document detailing the whole manufacturing process of C13H12N2O5S active pharmaceutical ingredient (API) in detail. Different forms of C13H12N2O5S DMFs exist exist since differing nations have different regulations, such as C13H12N2O5S USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A C13H12N2O5S DMF submitted to regulatory agencies in the US is known as a USDMF. C13H12N2O5S USDMF includes data on C13H12N2O5S's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The C13H12N2O5S USDMF is kept confidential to protect the manufacturer’s intellectual property.
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