Strength
750 mg/1
Manufacturer
ANI Pharmaceuticals, Inc.NDC
70954078510
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NABUMETONEApproval Type
Generic (ANDA)
FDA Application
ANDA219118On Market Since
1/7/2025
Pharmacological Classes
NABUMETONE 750 MG TABLET
Generic
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