FDA NDC Directory · JSON-LD · Markdown

Nabumetone

NDC 55700-840 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerQuality Care Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078420
Dosage form / routeTABLET · ORAL
Active ingredientsNABUMETONE (750 mg/1)
Marketing started20190626
Marketing ended20270531
Package count1

External sources

Source: openFDA. Public-domain (CC0).