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Aleve PM

NDC 0280-1200 · Bayer HealthCare LLC.

Generic nameDIPHENHYDRAMINE HYDROCHLORIDE and NAPROXEN SODIUM
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM
Strength25; 220 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryNDA

Packages

0280-1200-01 1 BOTTLE in 1 CARTON (0280-1200-01) / 120 TABLET, FILM COATED in 1 BOTTLE

0280-1200-02 2 TABLET, FILM COATED in 1 POUCH (0280-1200-02)

0280-1200-03 160 TABLET, FILM COATED in 1 BOTTLE (0280-1200-03)

0280-1200-04 1 BOTTLE in 1 CARTON (0280-1200-04) / 40 TABLET, FILM COATED in 1 BOTTLE

0280-1200-05 80 TABLET, FILM COATED in 1 BOTTLE (0280-1200-05)

0280-1200-08 1 BOTTLE in 1 CARTON (0280-1200-08) / 250 TABLET, FILM COATED in 1 BOTTLE

0280-1200-20 1 BOTTLE in 1 CARTON (0280-1200-20) / 20 TABLET, FILM COATED in 1 BOTTLE

0280-1200-40 1 BOTTLE in 1 CARTON (0280-1200-40) / 40 TABLET, FILM COATED in 1 BOTTLE

0280-1200-80 1 BOTTLE in 1 CARTON (0280-1200-80) / 80 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0135-7021 — acetaminophen and diphenhydramine HCl, 0280-0041 — Naproxen Sodium, 0280-0105 — Naproxen Sodium, 0280-0111 — NAPROXEN SODIUM, 0280-0112 — NAPROXEN SODIUM, 0280-0113 — NAPROXEN SODIUM, 0280-0114 — NAPROXEN SODIUM, 0280-0115 — NAPROXEN SODIUM, 0280-0130 — NAPROXEN SODIUM, 0280-0131 — NAPROXEN SODIUM, 0280-6000 — NAPROXEN SODIUM, 0280-6010 — NAPROXEN SODIUM, 0280-6020 — NAPROXEN SODIUM, 0280-6045 — naproxen sodium, pseudoephedrine hydrochloride, 0280-6050 — NAPROXEN SODIUM, 0280-6060 — NAPROXEN SODIUM, 0280-6070 — NAPROXEN SODIUM, 0280-6080 — Naproxen Sodium, 0280-6090 — naproxen sodium, pseudeoephedrine hydrochloride, 0280-6091 — Naproxen Sodium, +1347 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels