01 1Sumitomo Chemical
01 1CEFPIRAMIDE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6940
Submission : 1987-04-23
Status : Inactive
Type : II
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A Cefpiramide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefpiramide, including repackagers and relabelers. The FDA regulates Cefpiramide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefpiramide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cefpiramide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cefpiramide supplier is an individual or a company that provides Cefpiramide active pharmaceutical ingredient (API) or Cefpiramide finished formulations upon request. The Cefpiramide suppliers may include Cefpiramide API manufacturers, exporters, distributors and traders.
click here to find a list of Cefpiramide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Cefpiramide DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefpiramide active pharmaceutical ingredient (API) in detail. Different forms of Cefpiramide DMFs exist exist since differing nations have different regulations, such as Cefpiramide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cefpiramide DMF submitted to regulatory agencies in the US is known as a USDMF. Cefpiramide USDMF includes data on Cefpiramide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefpiramide USDMF is kept confidential to protect the manufacturer’s intellectual property.
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