# Naproxen sodium

NDC: 0480-0952
Generic name: naproxen sodium
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20221101

FDA application: ANDA075416

## Active ingredients

- NAPROXEN SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-0952"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-0952
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=826fd9e3-22fe-408b-820c-f2b710189555