# Naproxen Sodium

NDC: 59726-174
Generic name: Naproxen Sodium
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20180401
Marketing ended: 20261231
FDA application: ANDA208363

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59726-174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fc65fe79-c93b-4247-b9af-e562792a3e64