# Naproxen

NDC: 52817-381
Generic name: Naproxen
Labeler / Manufacturer: TruPharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230727

FDA application: ANDA216908

## 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:"52817-381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=004bb832-29d5-add0-e063-6394a90a90f4