01 1Ipca Laboratories
02 1Unichem Laboratories Limited
01 2BENDROFLUMETHIAZIDE USP
01 2India
01 1Active
02 1Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19857
Submission : 2006-11-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15847
Submission : 2002-02-04
Status : Active
Type : II
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A Flumesil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flumesil, including repackagers and relabelers. The FDA regulates Flumesil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flumesil 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 Flumesil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Flumesil supplier is an individual or a company that provides Flumesil active pharmaceutical ingredient (API) or Flumesil finished formulations upon request. The Flumesil suppliers may include Flumesil API manufacturers, exporters, distributors and traders.
click here to find a list of Flumesil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Flumesil DMF (Drug Master File) is a document detailing the whole manufacturing process of Flumesil active pharmaceutical ingredient (API) in detail. Different forms of Flumesil DMFs exist exist since differing nations have different regulations, such as Flumesil USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Flumesil DMF submitted to regulatory agencies in the US is known as a USDMF. Flumesil USDMF includes data on Flumesil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Flumesil USDMF is kept confidential to protect the manufacturer’s intellectual property.
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