01 1Daiichi Sankyo
01 1CEFMETAZOLE (FREE ACID)
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9887
Submission : 1982-09-03
Status : Inactive
Type : II
A Cefmetazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefmetazole, including repackagers and relabelers. The FDA regulates Cefmetazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefmetazole 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 Cefmetazole supplier is an individual or a company that provides Cefmetazole active pharmaceutical ingredient (API) or Cefmetazole finished formulations upon request. The Cefmetazole suppliers may include Cefmetazole API manufacturers, exporters, distributors and traders.
click here to find a list of Cefmetazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cefmetazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefmetazole active pharmaceutical ingredient (API) in detail. Different forms of Cefmetazole DMFs exist exist since differing nations have different regulations, such as Cefmetazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cefmetazole DMF submitted to regulatory agencies in the US is known as a USDMF. Cefmetazole USDMF includes data on Cefmetazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefmetazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cefmetazole suppliers with USDMF on PharmaCompass.
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