# NAPROXEN SODIUM

NDC: 41226-609
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: Kroger Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20210612

FDA application: ANDA090545

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"41226-609"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41226-609
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc185bf2-bc2c-f439-e053-2995a90a93d0