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01 1POLYTHIAZIDE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7777
Submission : 1988-11-18
Status : Inactive
Type : II
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A Polythiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polythiazide, including repackagers and relabelers. The FDA regulates Polythiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polythiazide 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 Polythiazide supplier is an individual or a company that provides Polythiazide active pharmaceutical ingredient (API) or Polythiazide finished formulations upon request. The Polythiazide suppliers may include Polythiazide API manufacturers, exporters, distributors and traders.
click here to find a list of Polythiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Polythiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of Polythiazide active pharmaceutical ingredient (API) in detail. Different forms of Polythiazide DMFs exist exist since differing nations have different regulations, such as Polythiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Polythiazide DMF submitted to regulatory agencies in the US is known as a USDMF. Polythiazide USDMF includes data on Polythiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Polythiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Polythiazide suppliers with USDMF on PharmaCompass.
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