FDA NDC Directory · JSON-LD · Markdown

BUPHENYL

NDC 75987-060 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namesodium phenylbutyrate
Labeler / ManufacturerHorizon Therapeutics USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020572
Dosage form / routeTABLET · ORAL
Active ingredientsSODIUM PHENYLBUTYRATE (500 mg/1)
Marketing started19960513
Package count1

External sources

Source: openFDA. Public-domain (CC0).