FDA NDC Directory · JSON-LD · Markdown

IBUPROFEN 250

NDC 73598-1104 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIBUPROFEN
Labeler / ManufacturerJHK Inc dba American Safety & First Aid
Marketing categoryAbbreviated NDA (generic) · App ANDA072096
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20000202
Package count1

External sources

Source: openFDA. Public-domain (CC0).