FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 69848-012 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20190701
Package count3

External sources

Source: openFDA. Public-domain (CC0).