# Naproxen Sodium

NDC: 55111-273
Generic name: Naproxen Sodium
Labeler / Manufacturer: Dr.Reddy's Laboratories Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 19980729

FDA application: ANDA075168

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-273"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-273
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aca5d497-fbc6-464d-2dee-25c50e11bc78