FDA NDC Directory · JSON-LD · Markdown

Nabumetone

NDC 76420-210 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (500 mg/1)
Marketing started20190626
Package count6

External sources

Source: openFDA. Public-domain (CC0).