# Naproxen

NDC: 59651-987
Generic name: Naproxen
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250508

FDA application: ANDA075390

## 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:"59651-987"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-987
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67815abd-5e97-4ccb-ac9b-28c2ef6123e7