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
- 63187-614_144ceffa-24aa-4423-ba09-1a6fa5c0d5cf
- Product NDC
- 63187-614
- 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 — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (63187-614-15) · 63187-614-15
- 20 TABLET in 1 BOTTLE (63187-614-20) · 63187-614-20
- 21 TABLET in 1 BOTTLE (63187-614-21) · 63187-614-21
- 28 TABLET in 1 BOTTLE (63187-614-28) · 63187-614-28
- 30 TABLET in 1 BOTTLE (63187-614-30) · 63187-614-30
- 40 TABLET in 1 BOTTLE (63187-614-40) · 63187-614-40
- 42 TABLET in 1 BOTTLE (63187-614-42) · 63187-614-42
- 45 TABLET in 1 BOTTLE (63187-614-45) · 63187-614-45
- 60 TABLET in 1 BOTTLE (63187-614-60) · 63187-614-60
- 90 TABLET in 1 BOTTLE (63187-614-90) · 63187-614-90
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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