United States · FDA National Drug Code directory
arthritis 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
- 41250-966_a80c0c5f-8bf9-4d1f-99cf-efd421d3db1a
- Product NDC
- 41250-966
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20070905
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-966-47) · 41250-966-47
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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