01 1RHODIA INC US 08512-7500 Cranbury
01 1ISOMETAMIDIAM
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 578
Submission : 1963-06-12
Status : Inactive
Type : II
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A Veridium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Veridium, including repackagers and relabelers. The FDA regulates Veridium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Veridium 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 Veridium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Veridium supplier is an individual or a company that provides Veridium active pharmaceutical ingredient (API) or Veridium finished formulations upon request. The Veridium suppliers may include Veridium API manufacturers, exporters, distributors and traders.
click here to find a list of Veridium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Veridium DMF (Drug Master File) is a document detailing the whole manufacturing process of Veridium active pharmaceutical ingredient (API) in detail. Different forms of Veridium DMFs exist exist since differing nations have different regulations, such as Veridium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Veridium DMF submitted to regulatory agencies in the US is known as a USDMF. Veridium USDMF includes data on Veridium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Veridium USDMF is kept confidential to protect the manufacturer’s intellectual property.
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