# naproxen sodium

NDC: 37808-713
Generic name: Naproxen Sodium
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20171003

FDA application: ANDA074661

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-713"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-713
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5dcf3df-2628-49c7-9d96-64886bebe631