01 1RHODIA INC US 08512-7500 Cranbury
01 1METHOTRIMEPRAZINE
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 577
Submission : 1963-06-12
Status : Inactive
Type : II
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A Nozinan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nozinan, including repackagers and relabelers. The FDA regulates Nozinan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nozinan 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 Nozinan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Nozinan supplier is an individual or a company that provides Nozinan active pharmaceutical ingredient (API) or Nozinan finished formulations upon request. The Nozinan suppliers may include Nozinan API manufacturers, exporters, distributors and traders.
click here to find a list of Nozinan suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Nozinan DMF (Drug Master File) is a document detailing the whole manufacturing process of Nozinan active pharmaceutical ingredient (API) in detail. Different forms of Nozinan DMFs exist exist since differing nations have different regulations, such as Nozinan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nozinan DMF submitted to regulatory agencies in the US is known as a USDMF. Nozinan USDMF includes data on Nozinan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nozinan USDMF is kept confidential to protect the manufacturer’s intellectual property.
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