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
50580-608_57301337-05f3-6afe-e063-6394a90aa4dd
Product NDC
50580-608
Form
TABLET, FILM COATED
Composition / generic term
acetaminophen and diphenhydramine hydrochloride
Labeler
Kenvue Brands LLC
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 BOTTLE in 1 CARTON (50580-608-01) / 24 TABLET, FILM COATED in 1 BOTTLE · 50580-608-01
  • 1 BOTTLE in 1 CARTON (50580-608-02) / 100 TABLET, FILM COATED in 1 BOTTLE · 50580-608-02
  • 1 BOTTLE in 1 CARTON (50580-608-03) / 150 TABLET, FILM COATED in 1 BOTTLE · 50580-608-03
  • 1 BOTTLE in 1 CARTON (50580-608-04) / 225 TABLET, FILM COATED in 1 BOTTLE · 50580-608-04
  • 2 TABLET, FILM COATED in 1 POUCH (50580-608-05) · 50580-608-05
  • 50 POUCH in 1 TRAY (50580-608-06) / 2 TABLET, FILM COATED in 1 POUCH · 50580-608-06
  • 2 POUCH in 1 CARTON (50580-608-07) / 2 TABLET, FILM COATED in 1 POUCH · 50580-608-07
  • 1 BOTTLE in 1 CARTON (50580-608-08) / 50 TABLET, FILM COATED in 1 BOTTLE · 50580-608-08

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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