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
- 72189-266_2c285455-94b8-8154-e063-6394a90a0e8c
- Product NDC
- 72189-266
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210916
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15) · 72189-266-15
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30) · 72189-266-30
- 40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40) · 72189-266-40
- 60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60) · 72189-266-60
- 100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71) · 72189-266-71
- 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72) · 72189-266-72
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90) · 72189-266-90
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 →