# naproxen sodium

NDC: 41250-818
Generic name: naproxen sodium
Labeler / Manufacturer: Meijer Distribution Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190326

FDA application: ANDA074661

## 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:"41250-818"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-818
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4e57560-ae89-4fc3-a66b-ebf3dc3f2448