01 1Ipca Laboratories
01 1FLUMEQUINE
01 1India
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10709
Submission : 1994-02-02
Status : Inactive
Type : II
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A Flumisol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumisol, including repackagers and relabelers. The FDA regulates Flumisol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumisol 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 Flumisol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flumisol supplier is an individual or a company that provides Flumisol active pharmaceutical ingredient (API) or Flumisol finished formulations upon request. The Flumisol suppliers may include Flumisol API manufacturers, exporters, distributors and traders.
click here to find a list of Flumisol suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Flumisol DMF (Drug Master File) is a document detailing the whole manufacturing process of Flumisol active pharmaceutical ingredient (API) in detail. Different forms of Flumisol DMFs exist exist since differing nations have different regulations, such as Flumisol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flumisol DMF submitted to regulatory agencies in the US is known as a USDMF. Flumisol USDMF includes data on Flumisol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flumisol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Flumisol suppliers with USDMF on PharmaCompass.
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