United States · FDA National Drug Code directory
Tylenol PM Extra Strength
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
- 85237-2945_55d0dd09-882d-754a-e063-6294a90a15ee
- Product NDC
- 85237-2945
- Form
- TABLET, FILM COATED
- Composition / generic term
- acetaminophen and diphenhydramine hydrochloride
- Labeler
- Select Consumer Group
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20160711
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 BLISTER PACK (85237-2945-1) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-1
- 2 POUCH in 1 BLISTER PACK (85237-2945-2) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-2
- 20 POUCH in 1 CONTAINER (85237-2945-3) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-3
- 25 POUCH in 1 CONTAINER (85237-2945-4) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-4
- 50 POUCH in 1 CONTAINER (85237-2945-6) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-6
- 3 POUCH in 1 BLISTER PACK (85237-2945-7) / 2 TABLET, FILM COATED in 1 POUCH (85237-2945-0) · 85237-2945-7
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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