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ibuprofen 200

NDC 0363-1517 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerWalgreen Company
Marketing categoryAbbreviated NDA (generic) · App ANDA077349
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20211020
Package count1

External sources

Source: openFDA. Public-domain (CC0).