01 1Atul Limited
01 1CLIOQUINOL
01 1India
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9078
Submission : 1991-04-20
Status : Inactive
Type : II
A Clioquinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clioquinol, including repackagers and relabelers. The FDA regulates Clioquinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clioquinol 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 Clioquinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Clioquinol supplier is an individual or a company that provides Clioquinol active pharmaceutical ingredient (API) or Clioquinol finished formulations upon request. The Clioquinol suppliers may include Clioquinol API manufacturers, exporters, distributors and traders.
click here to find a list of Clioquinol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clioquinol DMF (Drug Master File) is a document detailing the whole manufacturing process of Clioquinol active pharmaceutical ingredient (API) in detail. Different forms of Clioquinol DMFs exist exist since differing nations have different regulations, such as Clioquinol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Clioquinol DMF submitted to regulatory agencies in the US is known as a USDMF. Clioquinol USDMF includes data on Clioquinol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Clioquinol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Clioquinol suppliers with USDMF on PharmaCompass.
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