Discontinued
High Outlier
Strength
750 mg/1
Manufacturer
Almatica Pharma LLCNDC
52427027430
Classification
Brand
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
7/1/2017
Active Ingredients
NAPROXEN SODIUMApproval Type
New Drug (NDA)
FDA Application
NDA020353On Market Since
1/17/2014
Pharmacological Classes
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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