01 1Interpharma Praha AS
01 1IODIPAMIDE DRUG SUBSTANCE
01 1Czech Republic
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10576
Submission : 1993-11-18
Status : Inactive
Type : II
A Iodipamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iodipamide, including repackagers and relabelers. The FDA regulates Iodipamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iodipamide 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 Iodipamide supplier is an individual or a company that provides Iodipamide active pharmaceutical ingredient (API) or Iodipamide finished formulations upon request. The Iodipamide suppliers may include Iodipamide API manufacturers, exporters, distributors and traders.
click here to find a list of Iodipamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iodipamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Iodipamide active pharmaceutical ingredient (API) in detail. Different forms of Iodipamide DMFs exist exist since differing nations have different regulations, such as Iodipamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iodipamide DMF submitted to regulatory agencies in the US is known as a USDMF. Iodipamide USDMF includes data on Iodipamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iodipamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iodipamide suppliers with USDMF on PharmaCompass.
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