01 1RHODIA INC US 08512-7500 Cranbury
01 1DICHLOROPHEN (ANTHIPEN)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1163
Submission : 1968-04-10
Status : Inactive
Type : II
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A Korium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Korium, including repackagers and relabelers. The FDA regulates Korium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Korium 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 Korium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Korium supplier is an individual or a company that provides Korium active pharmaceutical ingredient (API) or Korium finished formulations upon request. The Korium suppliers may include Korium API manufacturers, exporters, distributors and traders.
click here to find a list of Korium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Korium DMF (Drug Master File) is a document detailing the whole manufacturing process of Korium active pharmaceutical ingredient (API) in detail. Different forms of Korium DMFs exist exist since differing nations have different regulations, such as Korium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Korium DMF submitted to regulatory agencies in the US is known as a USDMF. Korium USDMF includes data on Korium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Korium USDMF is kept confidential to protect the manufacturer’s intellectual property.
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