# Naproxen Sodium

NDC: 58602-819
Generic name: Naproxen Sodium
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20171211

FDA application: ANDA205497

## 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:"58602-819"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-819
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=46a15412-25d6-454d-86db-70321d19a2c9