# Leader All Day Pain Relief

NDC: 70000-0201
Generic name: Naproxen Sodium
Labeler / Manufacturer: Cardinal Health 110, LLC. dba Leader
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20161207

FDA application: ANDA074661

## 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:"70000-0201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70000-0201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b01c2b4e-a092-42dc-a387-d181d8ba14bb