FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 72189-231 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA090796
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (600 mg/1)
Marketing started20210604
Package count4

External sources

Source: openFDA. Public-domain (CC0).