FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 71335-3108 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA078329
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20200821
Package count1

External sources

Source: openFDA. Public-domain (CC0).