01 1RHODIA INC US 08512-7500 Cranbury
01 1DICHLOROPHEN (ANTHIPEN)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1163
Submission : 1968-04-10
Status : Inactive
Type : II
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A Trivex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trivex, including repackagers and relabelers. The FDA regulates Trivex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trivex 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 Trivex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Trivex supplier is an individual or a company that provides Trivex active pharmaceutical ingredient (API) or Trivex finished formulations upon request. The Trivex suppliers may include Trivex API manufacturers, exporters, distributors and traders.
click here to find a list of Trivex suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Trivex DMF (Drug Master File) is a document detailing the whole manufacturing process of Trivex active pharmaceutical ingredient (API) in detail. Different forms of Trivex DMFs exist exist since differing nations have different regulations, such as Trivex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trivex DMF submitted to regulatory agencies in the US is known as a USDMF. Trivex USDMF includes data on Trivex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trivex USDMF is kept confidential to protect the manufacturer’s intellectual property.
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