United States · FDA National Drug Code directory
Acetaminophen
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
- 79903-269_464fe735-09d4-88b8-e063-6394a90a1bc7
- Product NDC
- 79903-269
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- Walmart
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250116
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (79903-269-10) · 79903-269-10
- 225 TABLET in 1 BOTTLE (79903-269-22) · 79903-269-22
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →