01 1Bracco
01 1IOMEPROL
01 1Italy
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10299
Submission : 1993-06-15
Status : Inactive
Type : II
A Iomeprol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iomeprol, including repackagers and relabelers. The FDA regulates Iomeprol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iomeprol 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 Iomeprol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Iomeprol supplier is an individual or a company that provides Iomeprol active pharmaceutical ingredient (API) or Iomeprol finished formulations upon request. The Iomeprol suppliers may include Iomeprol API manufacturers, exporters, distributors and traders.
click here to find a list of Iomeprol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Iomeprol DMF (Drug Master File) is a document detailing the whole manufacturing process of Iomeprol active pharmaceutical ingredient (API) in detail. Different forms of Iomeprol DMFs exist exist since differing nations have different regulations, such as Iomeprol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iomeprol DMF submitted to regulatory agencies in the US is known as a USDMF. Iomeprol USDMF includes data on Iomeprol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iomeprol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Iomeprol suppliers with USDMF on PharmaCompass.
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