01 1Sifavitor srl
01 1TRICHLORMETHIAZIDE NF XIII
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2193
Submission : 1973-11-20
Status : Inactive
Type : II
20
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A Metahydrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metahydrin, including repackagers and relabelers. The FDA regulates Metahydrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metahydrin 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 Metahydrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Metahydrin supplier is an individual or a company that provides Metahydrin active pharmaceutical ingredient (API) or Metahydrin finished formulations upon request. The Metahydrin suppliers may include Metahydrin API manufacturers, exporters, distributors and traders.
click here to find a list of Metahydrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Metahydrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Metahydrin active pharmaceutical ingredient (API) in detail. Different forms of Metahydrin DMFs exist exist since differing nations have different regulations, such as Metahydrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Metahydrin DMF submitted to regulatory agencies in the US is known as a USDMF. Metahydrin USDMF includes data on Metahydrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Metahydrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
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