01 2Avanti Polar Lipids
01 1TRICAPRYLIN (730412)
02 1TRIOCTANOIN
01 2U.S.A
01 2Active
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31820
Submission : 2017-08-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12185
Submission : 1996-10-22
Status : Active
Type : II
A Tricaprylin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tricaprylin, including repackagers and relabelers. The FDA regulates Tricaprylin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tricaprylin 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 Tricaprylin supplier is an individual or a company that provides Tricaprylin active pharmaceutical ingredient (API) or Tricaprylin finished formulations upon request. The Tricaprylin suppliers may include Tricaprylin API manufacturers, exporters, distributors and traders.
click here to find a list of Tricaprylin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tricaprylin DMF (Drug Master File) is a document detailing the whole manufacturing process of Tricaprylin active pharmaceutical ingredient (API) in detail. Different forms of Tricaprylin DMFs exist exist since differing nations have different regulations, such as Tricaprylin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tricaprylin DMF submitted to regulatory agencies in the US is known as a USDMF. Tricaprylin USDMF includes data on Tricaprylin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tricaprylin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tricaprylin suppliers with USDMF on PharmaCompass.
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