Strength
500 mg/1
Manufacturer
Exelan Pharmaceuticals Inc.NDC
76282025705
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NABUMETONEApproval Type
Generic (ANDA)
FDA Application
ANDA078671On Market Since
4/14/2015
Pharmacological Classes
NABUMETONE 500 MG TABLET
Generic
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