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
- 71205-604_f49b4e82-120c-4012-b4b3-78c0f89ae8fd
- Product NDC
- 71205-604
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20081120
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (71205-604-15) · 71205-604-15
- 20 TABLET in 1 BOTTLE (71205-604-20) · 71205-604-20
- 21 TABLET in 1 BOTTLE (71205-604-21) · 71205-604-21
- 30 TABLET in 1 BOTTLE (71205-604-30) · 71205-604-30
- 40 TABLET in 1 BOTTLE (71205-604-40) · 71205-604-40
- 60 TABLET in 1 BOTTLE (71205-604-60) · 71205-604-60
- 90 TABLET in 1 BOTTLE (71205-604-90) · 71205-604-90
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 →