# Naproxen

NDC: 55700-888
Generic name: Naproxen
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210226
Marketing ended: 20270531
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:"55700-888"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-888
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1acfb8cc-6faf-4b3e-9304-4819c42de0a6
