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 NCGC00024910-01 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024910-01, including repackagers and relabelers. The FDA regulates NCGC00024910-01 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024910-01 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 NCGC00024910-01 supplier is an individual or a company that provides NCGC00024910-01 active pharmaceutical ingredient (API) or NCGC00024910-01 finished formulations upon request. The NCGC00024910-01 suppliers may include NCGC00024910-01 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024910-01 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A NCGC00024910-01 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00024910-01 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00024910-01 DMFs exist exist since differing nations have different regulations, such as NCGC00024910-01 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NCGC00024910-01 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00024910-01 USDMF includes data on NCGC00024910-01's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00024910-01 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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