01 1EDISON PHARMACEUTICALS INC
01 1ALPHA TOCOTRIENOL QUINONE (EPI-743)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22885
Submission : 2009-06-23
Status : Inactive
Type : II
A Vatiquinone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vatiquinone, including repackagers and relabelers. The FDA regulates Vatiquinone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vatiquinone 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 Vatiquinone supplier is an individual or a company that provides Vatiquinone active pharmaceutical ingredient (API) or Vatiquinone finished formulations upon request. The Vatiquinone suppliers may include Vatiquinone API manufacturers, exporters, distributors and traders.
click here to find a list of Vatiquinone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vatiquinone DMF (Drug Master File) is a document detailing the whole manufacturing process of Vatiquinone active pharmaceutical ingredient (API) in detail. Different forms of Vatiquinone DMFs exist exist since differing nations have different regulations, such as Vatiquinone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vatiquinone DMF submitted to regulatory agencies in the US is known as a USDMF. Vatiquinone USDMF includes data on Vatiquinone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vatiquinone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vatiquinone suppliers with USDMF on PharmaCompass.
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