01 1Yamasa Corporation
01 1DIQUAFOSOL TETRASODIUM
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14100
Submission : 1999-04-28
Status : Inactive
Type : II
A Diquafosol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diquafosol, including repackagers and relabelers. The FDA regulates Diquafosol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diquafosol 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 Diquafosol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diquafosol supplier is an individual or a company that provides Diquafosol active pharmaceutical ingredient (API) or Diquafosol finished formulations upon request. The Diquafosol suppliers may include Diquafosol API manufacturers, exporters, distributors and traders.
click here to find a list of Diquafosol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diquafosol DMF (Drug Master File) is a document detailing the whole manufacturing process of Diquafosol active pharmaceutical ingredient (API) in detail. Different forms of Diquafosol DMFs exist exist since differing nations have different regulations, such as Diquafosol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diquafosol DMF submitted to regulatory agencies in the US is known as a USDMF. Diquafosol USDMF includes data on Diquafosol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diquafosol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diquafosol suppliers with USDMF on PharmaCompass.
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