# Naproxen Sodium

NDC: 83324-109
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20250520

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:"83324-109"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83324-109
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=84b9e9a4-b805-420e-83be-ebe98776d1ee