01 1Medimpex
01 1VINPOCETINE (CAVITON R)
01 1United Kingdom
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3854
Submission : 1980-06-13
Status : Inactive
Type : II
A Vinpocetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vinpocetine, including repackagers and relabelers. The FDA regulates Vinpocetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vinpocetine 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 Vinpocetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vinpocetine supplier is an individual or a company that provides Vinpocetine active pharmaceutical ingredient (API) or Vinpocetine finished formulations upon request. The Vinpocetine suppliers may include Vinpocetine API manufacturers, exporters, distributors and traders.
click here to find a list of Vinpocetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vinpocetine DMF (Drug Master File) is a document detailing the whole manufacturing process of Vinpocetine active pharmaceutical ingredient (API) in detail. Different forms of Vinpocetine DMFs exist exist since differing nations have different regulations, such as Vinpocetine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vinpocetine DMF submitted to regulatory agencies in the US is known as a USDMF. Vinpocetine USDMF includes data on Vinpocetine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vinpocetine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vinpocetine suppliers with USDMF on PharmaCompass.
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