FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN

NDC 72476-112 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIbuprofen
Labeler / ManufacturerRETAIL BUSINESS SERVICES , LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA202312
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20200201
Package count2

External sources

Source: openFDA. Public-domain (CC0).