FDA NDC Directory · JSON-LD · Markdown

Oxaprozin

NDC 82804-261 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA075855
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXAPROZIN (600 mg/1)
Marketing started20010131
Package count1

External sources

Source: openFDA. Public-domain (CC0).