FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 61504-110 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIbuprofen
Labeler / ManufacturerAMERIFOODS TRADING COMPANY
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20231030
Package count1

External sources

Source: openFDA. Public-domain (CC0).