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
- 72189-231_2c285455-94b8-8154-e063-6394a90a0e8c
- Product NDC
- 72189-231
- Form
- TABLET, FILM COATED
- Composition / generic term
- IBUPROFEN
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210604
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21) · 72189-231-21
- 30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30) · 72189-231-30
- 60 TABLET, FILM COATED in 1 BOTTLE (72189-231-60) · 72189-231-60
- 90 TABLET, FILM COATED in 1 BOTTLE (72189-231-90) · 72189-231-90
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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