# Medique at Home Mediproxen

NDC: 47682-737
Generic name: Naproxen Sodium
Labeler / Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210201

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:"47682-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47682-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b591ba4f-d7d3-4c81-e053-2995a90a7c6e