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
- 56062-544_072ddb1b-cc26-41f9-be4b-993f99be6c02
- Product NDC
- 56062-544
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- Publix Super Markets Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071126
- 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 (56062-544-62) / 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE · 56062-544-62
- 1 BOTTLE in 1 CARTON (56062-544-78) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE · 56062-544-78
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.
Browse United States records →