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01 1BENZTHIAZIDE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8001
Submission : 1989-03-20
Status : Inactive
Type : II
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A Benzothiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzothiazide, including repackagers and relabelers. The FDA regulates Benzothiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzothiazide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Benzothiazide supplier is an individual or a company that provides Benzothiazide active pharmaceutical ingredient (API) or Benzothiazide finished formulations upon request. The Benzothiazide suppliers may include Benzothiazide API manufacturers, exporters, distributors and traders.
click here to find a list of Benzothiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Benzothiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of Benzothiazide active pharmaceutical ingredient (API) in detail. Different forms of Benzothiazide DMFs exist exist since differing nations have different regulations, such as Benzothiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Benzothiazide DMF submitted to regulatory agencies in the US is known as a USDMF. Benzothiazide USDMF includes data on Benzothiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Benzothiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Benzothiazide suppliers with USDMF on PharmaCompass.
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