FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 11673-991 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerTARGET CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA091239
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20200204
Package count5

External sources

Source: openFDA. Public-domain (CC0).