United States · FDA National Drug Code directory

Aleve 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
0280-1200_45265ccc-d985-a6ad-e063-6394a90a75b7
Product NDC
0280-1200
Form
TABLET, FILM COATED
Composition / generic term
DIPHENHYDRAMINE HYDROCHLORIDE and NAPROXEN SODIUM
Labeler
Bayer HealthCare LLC.
Marketing category
NDA
Marketing start / end (source format)
20140909
Source listing expiry
20261231

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 (0280-1200-01) / 120 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-01
  • 2 TABLET, FILM COATED in 1 POUCH (0280-1200-02) · 0280-1200-02
  • 160 TABLET, FILM COATED in 1 BOTTLE (0280-1200-03) · 0280-1200-03
  • 1 BOTTLE in 1 CARTON (0280-1200-04) / 40 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-04
  • 80 TABLET, FILM COATED in 1 BOTTLE (0280-1200-05) · 0280-1200-05
  • 1 BOTTLE in 1 CARTON (0280-1200-08) / 250 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-08
  • 1 BOTTLE in 1 CARTON (0280-1200-20) / 20 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-20
  • 1 BOTTLE in 1 CARTON (0280-1200-40) / 40 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-40
  • 1 BOTTLE in 1 CARTON (0280-1200-80) / 80 TABLET, FILM COATED in 1 BOTTLE · 0280-1200-80

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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