# Naproxen Sodium

NDC: 61504-145
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: AMERIFOODS TRADING COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20231030

FDA application: ANDA079096

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61504-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61504-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6dd2150-1643-18ff-e053-6294a90a422b