01 1Daiichi Sankyo
01 1CS-023 DRUG SUBSTANCE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17229
Submission : 2004-03-12
Status : Inactive
Type : II
A Cs 023 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cs 023, including repackagers and relabelers. The FDA regulates Cs 023 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cs 023 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 Cs 023 supplier is an individual or a company that provides Cs 023 active pharmaceutical ingredient (API) or Cs 023 finished formulations upon request. The Cs 023 suppliers may include Cs 023 API manufacturers, exporters, distributors and traders.
click here to find a list of Cs 023 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cs 023 DMF (Drug Master File) is a document detailing the whole manufacturing process of Cs 023 active pharmaceutical ingredient (API) in detail. Different forms of Cs 023 DMFs exist exist since differing nations have different regulations, such as Cs 023 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cs 023 DMF submitted to regulatory agencies in the US is known as a USDMF. Cs 023 USDMF includes data on Cs 023's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cs 023 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cs 023 suppliers with USDMF on PharmaCompass.
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