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Naproxen

NDC 70954-925 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218497
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsNAPROXEN (375 mg/1)
Marketing started20240613
Package count1

External sources

Source: openFDA. Public-domain (CC0).