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
- 68788-8531_0b5c32bc-2bff-491d-910b-7921c3395ef8
- Product NDC
- 68788-8531
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231006
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-8531-1) · 68788-8531-1
- 20 TABLET, FILM COATED in 1 BOTTLE (68788-8531-2) · 68788-8531-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-8531-3) · 68788-8531-3
- 14 TABLET, FILM COATED in 1 BOTTLE (68788-8531-4) · 68788-8531-4
- 50 TABLET, FILM COATED in 1 BOTTLE (68788-8531-5) · 68788-8531-5
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-8531-6) · 68788-8531-6
- 21 TABLET, FILM COATED in 1 BOTTLE (68788-8531-7) · 68788-8531-7
- 120 TABLET, FILM COATED in 1 BOTTLE (68788-8531-8) · 68788-8531-8
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-8531-9) · 68788-8531-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →