# Naproxen Sodium Diphenhydramine Hydrochloride

NDC: 21130-814
Generic name: Naproxen Sodium Diphenhydramine Hydrochloride
Labeler / Manufacturer: SAFEWAY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230630

FDA application: ANDA213663

## Active ingredients

- DIPHENHYDRAMINE HYDROCHLORIDE: 25 mg/1
- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-814"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-814
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ed0f3275-f156-13a3-e053-2a95a90a2ce8