FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 67296-2196 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRedpharm Drug
Marketing categoryAbbreviated NDA (generic) · App ANDA202413
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20240523
Package count2

External sources

Source: openFDA. Public-domain (CC0).