FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 0363-9594 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerWALGREENS CO.
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20211015
Package count2

External sources

Source: openFDA. Public-domain (CC0).