01 1Pfizer Inc
02 1SIGMA TAU
01 1CYCLOHEXIMIDE
02 1CYCLOHEXIMIDE (ACTIDIONE) U-4527
01 2U.S.A
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2497
Submission : 1975-07-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2830
Submission : 1976-12-30
Status : Inactive
Type : II
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A NSC 185 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NSC 185, including repackagers and relabelers. The FDA regulates NSC 185 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NSC 185 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 NSC 185 supplier is an individual or a company that provides NSC 185 active pharmaceutical ingredient (API) or NSC 185 finished formulations upon request. The NSC 185 suppliers may include NSC 185 API manufacturers, exporters, distributors and traders.
click here to find a list of NSC 185 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A NSC 185 DMF (Drug Master File) is a document detailing the whole manufacturing process of NSC 185 active pharmaceutical ingredient (API) in detail. Different forms of NSC 185 DMFs exist exist since differing nations have different regulations, such as NSC 185 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NSC 185 DMF submitted to regulatory agencies in the US is known as a USDMF. NSC 185 USDMF includes data on NSC 185's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NSC 185 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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