FDA NDC Directory · JSON-LD · Markdown

Cabinet Pain Reliever and Fever Reducer

NDC 68210-0026 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIbuprofen
Labeler / ManufacturerSpirit Pharmaceutical LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20191030
Package count2

External sources

Source: openFDA. Public-domain (CC0).