# basic care naproxen sodium pm

NDC: 72288-310
Generic name: diphenhydramine hydrochloride, naproxen sodium
Labeler / Manufacturer: Amazon.com Services LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210810

FDA application: ANDA208499

## 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:"72288-310"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72288-310
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7beed9e7-816b-494b-93fa-9caf10aa3834