FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 61919-463 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameIBUOROFEN
Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA091625
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20190822
Package count8

External sources

Source: openFDA. Public-domain (CC0).