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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