01 1Sumitomo Chemical
01 1SB210272
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10910
Submission : 1994-05-17
Status : Inactive
Type : II
A Sb 210232 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sb 210232, including repackagers and relabelers. The FDA regulates Sb 210232 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sb 210232 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 Sb 210232 supplier is an individual or a company that provides Sb 210232 active pharmaceutical ingredient (API) or Sb 210232 finished formulations upon request. The Sb 210232 suppliers may include Sb 210232 API manufacturers, exporters, distributors and traders.
click here to find a list of Sb 210232 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sb 210232 DMF (Drug Master File) is a document detailing the whole manufacturing process of Sb 210232 active pharmaceutical ingredient (API) in detail. Different forms of Sb 210232 DMFs exist exist since differing nations have different regulations, such as Sb 210232 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sb 210232 DMF submitted to regulatory agencies in the US is known as a USDMF. Sb 210232 USDMF includes data on Sb 210232's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sb 210232 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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