# All Day Pain Relief

NDC: 79903-005
Generic name: Naproxen Sodium
Labeler / Manufacturer: WALMART INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20201022

FDA application: ANDA204872

## 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:"79903-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79903-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4909e43-57ba-44bc-a234-a02cc884891c