# NAPROXEN

NDC: 72189-136
Generic name: NAPROXEN
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201015

FDA application: ANDA091416

## 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:"72189-136"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-136
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1b78c49-82e9-2402-e053-2a95a90ae35f