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01 1SULFAQUINOXALINE
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01 1Inactive
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4575
Submission : 1982-04-29
Status : Inactive
Type : II
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A Sulfaquinoxaline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfaquinoxaline, including repackagers and relabelers. The FDA regulates Sulfaquinoxaline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfaquinoxaline 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 Sulfaquinoxaline supplier is an individual or a company that provides Sulfaquinoxaline active pharmaceutical ingredient (API) or Sulfaquinoxaline finished formulations upon request. The Sulfaquinoxaline suppliers may include Sulfaquinoxaline API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfaquinoxaline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulfaquinoxaline DMF (Drug Master File) is a document detailing the whole manufacturing process of Sulfaquinoxaline active pharmaceutical ingredient (API) in detail. Different forms of Sulfaquinoxaline DMFs exist exist since differing nations have different regulations, such as Sulfaquinoxaline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sulfaquinoxaline DMF submitted to regulatory agencies in the US is known as a USDMF. Sulfaquinoxaline USDMF includes data on Sulfaquinoxaline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sulfaquinoxaline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sulfaquinoxaline suppliers with USDMF on PharmaCompass.
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