# Naproxen sodium

NDC: 69230-329
Generic name: Naproxen sodium
Labeler / Manufacturer: Camber Consumer Care Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221028

FDA application: ANDA211065

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69230-329"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69230-329
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1008e19-ff0d-4ed2-909d-bae5a82a1234