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
- 68788-4139_c0156053-add5-4bd5-b89f-f90df2e73be4
- Product NDC
- 68788-4139
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260706
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-4139-1) · 68788-4139-1
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-4139-3) · 68788-4139-3
- 50 TABLET, FILM COATED in 1 BOTTLE (68788-4139-5) · 68788-4139-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-4139-6) · 68788-4139-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-4139-9) · 68788-4139-9
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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