FDA NDC Directory · JSON-LD · Markdown

Uline Ibuprofen

NDC 69790-609 · HUMAN OTC DRUG · TABLET, COATED

Generic nameIbuprofen
Labeler / ManufacturerUline
Marketing categoryAbbreviated NDA (generic) · App ANDA075010
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20220404
Package count1

External sources

Source: openFDA. Public-domain (CC0).