01 1Ashland
01 18-HYDROXYQUINOLINE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2071
Submission : 1973-01-31
Status : Inactive
Type : II
A Oxyquinoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxyquinoline, including repackagers and relabelers. The FDA regulates Oxyquinoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxyquinoline 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 Oxyquinoline supplier is an individual or a company that provides Oxyquinoline active pharmaceutical ingredient (API) or Oxyquinoline finished formulations upon request. The Oxyquinoline suppliers may include Oxyquinoline API manufacturers, exporters, distributors and traders.
click here to find a list of Oxyquinoline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxyquinoline DMF (Drug Master File) is a document detailing the whole manufacturing process of Oxyquinoline active pharmaceutical ingredient (API) in detail. Different forms of Oxyquinoline DMFs exist exist since differing nations have different regulations, such as Oxyquinoline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Oxyquinoline DMF submitted to regulatory agencies in the US is known as a USDMF. Oxyquinoline USDMF includes data on Oxyquinoline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Oxyquinoline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Oxyquinoline suppliers with USDMF on PharmaCompass.
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