FDA NDC Directory · JSON-LD · Markdown

VALUMEDS IBUPROFEN

NDC 68210-0800 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameIBUPROFEN
Labeler / ManufacturerSPIRIT PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091239
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
Marketing started20170519
Package count2

External sources

Source: openFDA. Public-domain (CC0).