United States · FDA National Drug Code directory
Ibuprofen
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
- 72189-556_4c4c7dc3-d5c8-f3d9-e063-6294a90a426f
- Product NDC
- 72189-556
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240611
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (72189-556-20) · 72189-556-20
- 21 TABLET in 1 BOTTLE (72189-556-21) · 72189-556-21
- 30 TABLET in 1 BOTTLE (72189-556-30) · 72189-556-30
- 40 TABLET in 1 BOTTLE (72189-556-40) · 72189-556-40
- 45 TABLET in 1 BOTTLE (72189-556-45) · 72189-556-45
- 60 TABLET in 1 BOTTLE (72189-556-60) · 72189-556-60
- 100 TABLET in 1 BOTTLE (72189-556-71) · 72189-556-71
- 90 TABLET in 1 BOTTLE (72189-556-90) · 72189-556-90
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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