FDA NDC Directory · JSON-LD · Markdown

Ibuprofen

NDC 50090-2597 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA091625
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (800 mg/1)
Marketing started20151221
Package count1

External sources

Source: openFDA. Public-domain (CC0).