# NAPROXEN SODIUM

NDC: 57344-145
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: AAA Pharmaceutical, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20120401

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:"57344-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57344-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5ea3217d-845d-4781-b849-6b00babdc214