FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 0363-9612 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerWALGREENS
Marketing categoryAbbreviated NDA (generic) · App ANDA091237
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20181211
Package count4

External sources

Source: openFDA. Public-domain (CC0).