01 1Eisai
01 1MENFEGOL
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6008
Submission : 1985-06-28
Status : Inactive
Type : II
A Menfegol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menfegol, including repackagers and relabelers. The FDA regulates Menfegol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menfegol 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 Menfegol supplier is an individual or a company that provides Menfegol active pharmaceutical ingredient (API) or Menfegol finished formulations upon request. The Menfegol suppliers may include Menfegol API manufacturers, exporters, distributors and traders.
click here to find a list of Menfegol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Menfegol DMF (Drug Master File) is a document detailing the whole manufacturing process of Menfegol active pharmaceutical ingredient (API) in detail. Different forms of Menfegol DMFs exist exist since differing nations have different regulations, such as Menfegol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Menfegol DMF submitted to regulatory agencies in the US is known as a USDMF. Menfegol USDMF includes data on Menfegol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Menfegol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Menfegol suppliers with USDMF on PharmaCompass.
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