OTC
Strength
220 mg/1
Manufacturer
Chain Drug Marketing AssociationNDC
63868046501
Classification
Generic
Dosage Form
TABLET, COATED
Route
ORAL
Last Updated
6/21/2023
Active Ingredients
NAPROXEN SODIUMApproval Type
Generic (ANDA)
FDA Application
ANDA079096On Market Since
9/3/2009
Pharmacological Classes
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