# Naproxen Sodium

NDC: 37808-049
Generic name: Naproxen Sodium
Labeler / Manufacturer: HEB
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20190101

FDA application: NDA021920

## 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:"37808-049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df8ea301-c48b-4da4-9e8e-5c69cac6cba7