FDA NDC Directory · JSON-LD · Markdown

Nabumetone

NDC 60687-630 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078671
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNABUMETONE (500 mg/1)
Marketing started20220323
Package count1

External sources

Source: openFDA. Public-domain (CC0).