# Naproxen

NDC: 71205-597
Generic name: Naproxen
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200301

FDA application: ANDA212517

## 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:"71205-597"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-597
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0670241-f1f9-4fdf-83d4-547e7b800811