01 1Mallinckrodt Pharmaceuticals
01 1OPTIMARK(R) (GADOVERSETAMIDE INJECTION) PARAMETRIC RELEASE
01 1Ireland
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17360
Submission : 2004-06-23
Status : Inactive
Type : II
A Gadoversetamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gadoversetamide, including repackagers and relabelers. The FDA regulates Gadoversetamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gadoversetamide 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 Gadoversetamide supplier is an individual or a company that provides Gadoversetamide active pharmaceutical ingredient (API) or Gadoversetamide finished formulations upon request. The Gadoversetamide suppliers may include Gadoversetamide API manufacturers, exporters, distributors and traders.
click here to find a list of Gadoversetamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gadoversetamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Gadoversetamide active pharmaceutical ingredient (API) in detail. Different forms of Gadoversetamide DMFs exist exist since differing nations have different regulations, such as Gadoversetamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gadoversetamide DMF submitted to regulatory agencies in the US is known as a USDMF. Gadoversetamide USDMF includes data on Gadoversetamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gadoversetamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gadoversetamide suppliers with USDMF on PharmaCompass.
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