FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 68016-635 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerChain Drug Consortium
Marketing categoryAbbreviated NDA (generic) · App ANDA075139
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started19990301
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).