# Naproxen Sodium

NDC: 67091-140
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: WinCo Foods, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20141215

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:"67091-140"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67091-140
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=074fc2b9-743b-458e-a0c0-d5f27633bbf3