# Naproxen

NDC: 80425-0049
Generic name: Naproxen
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100218

FDA application: ANDA075927

## Active ingredients

- NAPROXEN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af9a94a8-3825-eabd-e053-2a95a90acd58