01 1Sumitomo Pharma
01 1AT-4140
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8375
Submission : 1990-01-16
Status : Inactive
Type : II
A Sparfloxacin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sparfloxacin, including repackagers and relabelers. The FDA regulates Sparfloxacin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sparfloxacin 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 Sparfloxacin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sparfloxacin supplier is an individual or a company that provides Sparfloxacin active pharmaceutical ingredient (API) or Sparfloxacin finished formulations upon request. The Sparfloxacin suppliers may include Sparfloxacin API manufacturers, exporters, distributors and traders.
click here to find a list of Sparfloxacin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sparfloxacin DMF (Drug Master File) is a document detailing the whole manufacturing process of Sparfloxacin active pharmaceutical ingredient (API) in detail. Different forms of Sparfloxacin DMFs exist exist since differing nations have different regulations, such as Sparfloxacin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sparfloxacin DMF submitted to regulatory agencies in the US is known as a USDMF. Sparfloxacin USDMF includes data on Sparfloxacin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sparfloxacin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sparfloxacin suppliers with USDMF on PharmaCompass.
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