United States · FDA National Drug Code directory
IBU
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
- 67296-0913_3251a7a8-7561-cf22-e063-6394a90adcb3
- Product NDC
- 67296-0913
- Form
- TABLET
- Composition / generic term
- IBU
- Labeler
- RedPharm Drug, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081120
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (67296-0913-1) · 67296-0913-1
- 10 TABLET in 1 BOTTLE (67296-0913-3) · 67296-0913-3
- 90 TABLET in 1 BOTTLE (67296-0913-9) · 67296-0913-9
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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