# All Day Pain Relief

NDC: 59428-604
Generic name: Naproxen Sodium
Labeler / Manufacturer: Zapotol Products Corp
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:"59428-604"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59428-604
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c422d300-3f4e-4121-8eaf-56683911b884