01 1Eastman Chemical Company
01 1TRIACETIN (PLASTICIZER) USP
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11292
Submission : 1995-01-05
Status : Inactive
Type : IV
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A Triacetina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triacetina, including repackagers and relabelers. The FDA regulates Triacetina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triacetina 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 Triacetina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Triacetina supplier is an individual or a company that provides Triacetina active pharmaceutical ingredient (API) or Triacetina finished formulations upon request. The Triacetina suppliers may include Triacetina API manufacturers, exporters, distributors and traders.
click here to find a list of Triacetina suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Triacetina DMF (Drug Master File) is a document detailing the whole manufacturing process of Triacetina active pharmaceutical ingredient (API) in detail. Different forms of Triacetina DMFs exist exist since differing nations have different regulations, such as Triacetina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Triacetina DMF submitted to regulatory agencies in the US is known as a USDMF. Triacetina USDMF includes data on Triacetina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Triacetina USDMF is kept confidential to protect the manufacturer’s intellectual property.
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