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
- 79481-0423_65d1d017-6a03-477d-bb35-98d606a8036c
- Product NDC
- 79481-0423
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Meijer, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240715
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (79481-0423-0) / 24 TABLET, FILM COATED in 1 BOTTLE · 79481-0423-0
- 1 BOTTLE in 1 CARTON (79481-0423-1) / 50 TABLET, FILM COATED in 1 BOTTLE · 79481-0423-1
- 500 TABLET, FILM COATED in 1 BOTTLE (79481-0423-2) · 79481-0423-2
- 1 BOTTLE in 1 CARTON (79481-0423-3) / 100 TABLET, FILM COATED in 1 BOTTLE · 79481-0423-3
- 2 BOTTLE in 1 CARTON (79481-0423-4) / 100 TABLET, FILM COATED in 1 BOTTLE · 79481-0423-4
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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