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Buphenyl

NDC 75987-070 · HUMAN PRESCRIPTION DRUG · POWDER

Generic namesodium phenylbutyrate
Labeler / ManufacturerHorizon Therapeutics USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020573
Dosage form / routePOWDER · ORAL
Active ingredientsSODIUM PHENYLBUTYRATE (.94 g/g)
Marketing started19960430
Package count1

External sources

Source: openFDA. Public-domain (CC0).