FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 68016-645 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerChain Drug Consortium
Marketing categoryAbbreviated NDA (generic) · App ANDA075010
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19880524
Marketing ended20260831
Package count3

External sources

Source: openFDA. Public-domain (CC0).