# All Day Pain Relief

NDC: 79903-389
Generic name: Naproxen Sodium
Labeler / Manufacturer: Walmart Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250510

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:"79903-389"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79903-389
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32df7378-4dd1-4f7e-e063-6394a90ad948