01 1Kyowa Hakko Bio
01 1KW-2189 DRUG SUBSTANCE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12420
Submission : 1997-03-18
Status : Inactive
Type : II
A Chembl2106438 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chembl2106438, including repackagers and relabelers. The FDA regulates Chembl2106438 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chembl2106438 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 Chembl2106438 supplier is an individual or a company that provides Chembl2106438 active pharmaceutical ingredient (API) or Chembl2106438 finished formulations upon request. The Chembl2106438 suppliers may include Chembl2106438 API manufacturers, exporters, distributors and traders.
click here to find a list of Chembl2106438 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chembl2106438 DMF (Drug Master File) is a document detailing the whole manufacturing process of Chembl2106438 active pharmaceutical ingredient (API) in detail. Different forms of Chembl2106438 DMFs exist exist since differing nations have different regulations, such as Chembl2106438 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Chembl2106438 DMF submitted to regulatory agencies in the US is known as a USDMF. Chembl2106438 USDMF includes data on Chembl2106438's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Chembl2106438 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Chembl2106438 suppliers with USDMF on PharmaCompass.
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