# All Day Back and Muscle Pain Relief

NDC: 79903-609
Generic name: Naproxen sodium
Labeler / Manufacturer: Walmart Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20231215

FDA application: ANDA090545

## 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:"79903-609"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79903-609
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=062b9ffe-b4fc-9f5a-e063-6294a90a560e