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
- 79903-132_a3731272-35ef-4fb8-aeb2-3421f68f715a
- Product NDC
- 79903-132
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- WALMART INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220726
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 325 TABLET, EXTENDED RELEASE in 1 BOTTLE (79903-132-25) · 79903-132-25
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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