01 1Aarti Drugs
02 1Procos
01 2NIMESULIDE
01 1India
02 1Italy
01 2Inactive
01 2Blank
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
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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, and more, enabling you to easily find the right Nimesulide manufacturer or Nimesulide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nimesulide manufacturer or Nimesulide supplier.
A Nimesil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nimesil, including repackagers and relabelers. The FDA regulates Nimesil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nimesil 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 Nimesil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nimesil supplier is an individual or a company that provides Nimesil active pharmaceutical ingredient (API) or Nimesil finished formulations upon request. The Nimesil suppliers may include Nimesil API manufacturers, exporters, distributors and traders.
click here to find a list of Nimesil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Nimesil DMF (Drug Master File) is a document detailing the whole manufacturing process of Nimesil active pharmaceutical ingredient (API) in detail. Different forms of Nimesil DMFs exist exist since differing nations have different regulations, such as Nimesil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nimesil DMF submitted to regulatory agencies in the US is known as a USDMF. Nimesil USDMF includes data on Nimesil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nimesil USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Nimesil suppliers with USDMF on PharmaCompass.
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