High Outlier
Strength
500 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00480095258
Classification
Generic
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
NAPROXEN SODIUMApproval Type
Generic (ANDA)
FDA Application
ANDA075416On Market Since
11/1/2022
Pharmacological Classes
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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