FDA NDC Directory · JSON-LD · Markdown

pain relief ibuprofen

NDC 11822-0392 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerRite Aid Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA075139
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20020330
Package count2

External sources

Source: openFDA. Public-domain (CC0).