FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 30142-517 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerKroger Company
Marketing categoryAbbreviated NDA (generic) · App ANDA077349
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20060427
Package count1

External sources

Source: openFDA. Public-domain (CC0).