FDA NDC Directory · JSON-LD · Markdown

Nabumetone

NDC 68788-7597 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (750 mg/1)
Marketing started20200213
Package count6

External sources

Source: openFDA. Public-domain (CC0).