# Naproxen Sodium

NDC: 50844-417
Generic name: Naproxen Sodium
Labeler / Manufacturer: L.N.K. International, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170201

FDA application: ANDA204872

## 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:"50844-417"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-417
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=717518e4-2537-4229-b765-c6acfe963d4b