FDA NDC Directory · JSON-LD · Markdown

NABUMETONE

NDC 72189-184 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / Manufacturerdirect rx
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (500 mg/1)
Marketing started20210511
Package count4

External sources

Source: openFDA. Public-domain (CC0).