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
- 53329-643_4f1bbf5a-3e39-3618-e063-6394a90ac6c8
- Product NDC
- 53329-643
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- Medline Industries, LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020430 / 20261231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53329-643-29) · 53329-643-29
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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