FDA NDC Directory · JSON-LD · Markdown

up and up ibuprofen

NDC 11673-685 · HUMAN OTC DRUG · SUSPENSION

Generic nameIbuprofen
Labeler / ManufacturerTarget Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA074937
Dosage form / routeSUSPENSION · ORAL
Active ingredientsIBUPROFEN (100 mg/5mL)
Marketing started20090710
Package count2

External sources

Source: openFDA. Public-domain (CC0).