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01 1PENTEX HUMAN TRANSFERRIN, IRON SATURATED
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9256
Submission : 1991-07-24
Status : Inactive
Type : II
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A Uric Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uric Acid, including repackagers and relabelers. The FDA regulates Uric Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uric Acid 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 Uric Acid supplier is an individual or a company that provides Uric Acid active pharmaceutical ingredient (API) or Uric Acid finished formulations upon request. The Uric Acid suppliers may include Uric Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Uric Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Uric Acid DMF (Drug Master File) is a document detailing the whole manufacturing process of Uric Acid active pharmaceutical ingredient (API) in detail. Different forms of Uric Acid DMFs exist exist since differing nations have different regulations, such as Uric Acid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Uric Acid DMF submitted to regulatory agencies in the US is known as a USDMF. Uric Acid USDMF includes data on Uric Acid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Uric Acid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Uric Acid suppliers with USDMF on PharmaCompass.
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