FDA NDC Directory · JSON-LD · Markdown

Nabumetone

NDC 70518-4047 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (750 mg/1)
Marketing started20240407
Package count3

External sources

Source: openFDA. Public-domain (CC0).