FDA NDC Directory · JSON-LD · Markdown

ibuprofen

NDC 51672-5321 · HUMAN OTC DRUG · SUSPENSION

Labeler / ManufacturerTARO PHARMACEUTICALS U.S.A., INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA211666
Dosage form / routeSUSPENSION · ORAL
Active ingredientsIBUPROFEN (100 mg/5mL)
Marketing started20240815
Package count2

External sources

Source: openFDA. Public-domain (CC0).