United States · FDA National Drug Code directory
Pain Relief
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
- 41250-802_ca8b0135-3528-4821-8b8d-6cd3d1757606
- Product NDC
- 41250-802
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170303
- 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 (41250-802-62) / 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE · 41250-802-62
- 1 BOTTLE in 1 CARTON (41250-802-78) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE · 41250-802-78
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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