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Naprelan

NDC 52427-273 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameNaproxen Sodium
Labeler / ManufacturerAlmatica Pharma LLC
Marketing categoryNew Drug Application (innovator) · App NDA020353
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNAPROXEN SODIUM (500 mg/1)
Marketing started20140117
Marketing ended20270701
Package count1

External sources

Source: openFDA. Public-domain (CC0).