# Naproxen

NDC: 68788-7572
Generic name: Naproxen Sodium
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190101

FDA application: ANDA204872

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-7572"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7572
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20eb9d9f-11df-464f-a1b0-949f8fda4042