United States · FDA National Drug Code directory
PANADOL 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
- 0135-7011_10c12d49-cd3c-e104-e063-6294a90a4e5a
- Product NDC
- 0135-7011
- Form
- TABLET, FILM COATED
- Composition / generic term
- acetaminophen
- Labeler
- Haleon US Holdings LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20210215
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 POUCH (0135-7011-01) · 0135-7011-01
- 1 BOTTLE in 1 CARTON (0135-7011-02) / 24 TABLET, FILM COATED in 1 BOTTLE · 0135-7011-02
- 1 BOTTLE in 1 CARTON (0135-7011-03) / 50 TABLET, FILM COATED in 1 BOTTLE · 0135-7011-03
- 1 BOTTLE in 1 CARTON (0135-7011-04) / 100 TABLET, FILM COATED in 1 BOTTLE · 0135-7011-04
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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