01 1Fujifilm Diosynth Biotechnologies
01 1TRENBOLONE ACETATE
01 1United Kingdom
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16347
Submission : 2003-01-03
Status : Inactive
Type : II
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A Finaplix H manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Finaplix H, including repackagers and relabelers. The FDA regulates Finaplix H manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Finaplix H 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 Finaplix H manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Finaplix H supplier is an individual or a company that provides Finaplix H active pharmaceutical ingredient (API) or Finaplix H finished formulations upon request. The Finaplix H suppliers may include Finaplix H API manufacturers, exporters, distributors and traders.
click here to find a list of Finaplix H suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Finaplix H DMF (Drug Master File) is a document detailing the whole manufacturing process of Finaplix H active pharmaceutical ingredient (API) in detail. Different forms of Finaplix H DMFs exist exist since differing nations have different regulations, such as Finaplix H USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Finaplix H DMF submitted to regulatory agencies in the US is known as a USDMF. Finaplix H USDMF includes data on Finaplix H's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Finaplix H USDMF is kept confidential to protect the manufacturer’s intellectual property.
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