# ALL DAY PAIN RELIEF

NDC: 0363-9608
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: WALGREENS
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20190626

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:"0363-9608"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9608
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8771b84f-47bf-116c-e053-2995a90a0aad