FDA NDC Directory · JSON-LD · Markdown

IBU

NDC 55111-684 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameIbuprofen
Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075682
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20081120
Package count6

External sources

Source: openFDA. Public-domain (CC0).