FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 37808-709 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA077349
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20060704
Package count1

External sources

Source: openFDA. Public-domain (CC0).