FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN Immediate Release

NDC 59556-857 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIBUPROFEN
Labeler / ManufacturerStrides Pharma Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA079129
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20220318
Package count2

External sources

Source: openFDA. Public-domain (CC0).