# ALL NIGHT PAIN RELIEF PM

NDC: 0363-2264
Generic name: diphenhydramine hydrochloride, naproxen sodium
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260427

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:"0363-2264"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-2264
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43e4ed28-b1be-4548-86ac-f40f9f83f04e