FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 51672-1385 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209204
Dosage form / routeSUSPENSION · ORAL
Active ingredientsIBUPROFEN (100 mg/5mL)
Marketing started20170623
Package count2

External sources

Source: openFDA. Public-domain (CC0).