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
- 68788-8354_72ece265-2379-46ed-8f63-4d24bae4932a
- Product NDC
- 68788-8354
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230210
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (68788-8354-1) · 68788-8354-1
- 20 TABLET in 1 BOTTLE (68788-8354-2) · 68788-8354-2
- 30 TABLET in 1 BOTTLE (68788-8354-3) · 68788-8354-3
- 14 TABLET in 1 BOTTLE (68788-8354-4) · 68788-8354-4
- 50 TABLET in 1 BOTTLE (68788-8354-5) · 68788-8354-5
- 60 TABLET in 1 BOTTLE (68788-8354-6) · 68788-8354-6
- 21 TABLET in 1 BOTTLE (68788-8354-7) · 68788-8354-7
- 120 TABLET in 1 BOTTLE (68788-8354-8) · 68788-8354-8
- 90 TABLET in 1 BOTTLE (68788-8354-9) · 68788-8354-9
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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