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