# All Day Relief

NDC: 56062-368
Generic name: Naproxen Sodium
Labeler / Manufacturer: Publix Super Markets Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19971229

FDA application: ANDA074661

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"56062-368"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=56062-368
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=688451a2-e94a-434a-8e9c-9fe3abf5c3d5