United States · FDA National Drug Code directory

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A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0363-2264_81c4f94d-6f5e-4e69-940b-b94b3533963c
Product NDC
0363-2264
Form
TABLET, FILM COATED
Composition / generic term
diphenhydramine hydrochloride, naproxen sodium
Labeler
Walgreen Company
Marketing category
ANDA
Marketing start / end (source format)
20260427
Source listing expiry
20271231

Source-listed ingredients

  • DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0363-2264-27) / 80 TABLET, FILM COATED in 1 BOTTLE (0363-2264-80) · 0363-2264-27

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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