FDA NDC Directory · JSON-LD · Markdown

RIGHT REMEDIES Ibuprofen 200 MG

NDC 70692-179 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerStrive Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079129
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20250923
Package count1

External sources

Source: openFDA. Public-domain (CC0).