United States · FDA National Drug Code directory
naproxen sodium pm
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
- 41250-526_a1f7704d-079a-4eac-b0d1-cf953e50fd1e
- Product NDC
- 41250-526
- Form
- TABLET, FILM COATED
- Composition / generic term
- diphenhydramine hydrochloride, naproxen sodium
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200114
- 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 (41250-526-27) / 80 TABLET, FILM COATED in 1 BOTTLE · 41250-526-27
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →