United States · FDA National Drug Code directory
Acetaminophen Extended-Release Tablets, 650 mg
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
- 25000-071_9e2c09cd-1bd4-4a86-8911-ba904d8a76cb
- Product NDC
- 25000-071
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210902
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (25000-071-02) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE · 25000-071-02
- 1 BOTTLE in 1 CARTON (25000-071-08) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE · 25000-071-08
- 1 BOTTLE in 1 CARTON (25000-071-10) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE · 25000-071-10
- 1 BOTTLE in 1 CARTON (25000-071-11) / 290 TABLET, EXTENDED RELEASE in 1 BOTTLE · 25000-071-11
- 400 TABLET, EXTENDED RELEASE in 1 BOTTLE (25000-071-45) · 25000-071-45
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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