# Medique Mediproxen

NDC: 47682-237
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: 20081230

FDA application: ANDA079096

## 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:"47682-237"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47682-237
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6261d45-df1f-483b-b013-3cd6f78d9d43