01 1Sumitomo Pharma
01 1SMP-797 DRUG SUBSTANCE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18146
Submission : 2005-03-02
Status : Inactive
Type : II
A Smp 797 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Smp 797, including repackagers and relabelers. The FDA regulates Smp 797 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Smp 797 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 Smp 797 supplier is an individual or a company that provides Smp 797 active pharmaceutical ingredient (API) or Smp 797 finished formulations upon request. The Smp 797 suppliers may include Smp 797 API manufacturers, exporters, distributors and traders.
click here to find a list of Smp 797 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Smp 797 DMF (Drug Master File) is a document detailing the whole manufacturing process of Smp 797 active pharmaceutical ingredient (API) in detail. Different forms of Smp 797 DMFs exist exist since differing nations have different regulations, such as Smp 797 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Smp 797 DMF submitted to regulatory agencies in the US is known as a USDMF. Smp 797 USDMF includes data on Smp 797's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Smp 797 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Smp 797 suppliers with USDMF on PharmaCompass.
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