FDA NDC Directory · JSON-LD · Markdown

Fast Pain Relief

NDC 69517-111 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIbuprofen
Labeler / ManufacturerHealthLife of USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079174
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20110101
Package count4

External sources

Source: openFDA. Public-domain (CC0).