01 1Daiichi Sankyo
02 1UBE Industries
01 1CS-615 DRUG PRODUCT
02 1CS-615 DRUG SUBSTANCE
01 2Japan
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13280
Submission : 1998-10-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13273
Submission : 1998-10-14
Status : Inactive
Type : II
14
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A DSSTox_CID_3719 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3719, including repackagers and relabelers. The FDA regulates DSSTox_CID_3719 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3719 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 DSSTox_CID_3719 supplier is an individual or a company that provides DSSTox_CID_3719 active pharmaceutical ingredient (API) or DSSTox_CID_3719 finished formulations upon request. The DSSTox_CID_3719 suppliers may include DSSTox_CID_3719 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3719 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A DSSTox_CID_3719 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_3719 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_3719 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_3719 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSSTox_CID_3719 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_3719 USDMF includes data on DSSTox_CID_3719's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_3719 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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