FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 70512-780 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameibuprofen
Labeler / ManufacturerSOLA Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078329
Dosage form / routeTABLET · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20241201
Package count2

External sources

Source: openFDA. Public-domain (CC0).