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
41250-658_24353a73-4f9e-68ba-e063-6394a90ac0b2
Product NDC
41250-658
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Acetaminophen
Labeler
Meijer
Marketing category
ANDA
Marketing start / end (source format)
20200306 / 20261130

Source-listed ingredients

  • ACETAMINOPHEN — 650 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, PLASTIC in 1 CARTON (41250-658-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC · 41250-658-03

Source and coverage

Open FDA National Drug Code directory

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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