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
- 63187-022_7db62aa5-dd71-4f62-b656-c4df75686f02
- Product NDC
- 63187-022
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20091123
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET in 1 BOTTLE (63187-022-15) · 63187-022-15
- 20 TABLET in 1 BOTTLE (63187-022-20) · 63187-022-20
- 21 TABLET in 1 BOTTLE (63187-022-21) · 63187-022-21
- 30 TABLET in 1 BOTTLE (63187-022-30) · 63187-022-30
- 40 TABLET in 1 BOTTLE (63187-022-40) · 63187-022-40
- 45 TABLET in 1 BOTTLE (63187-022-45) · 63187-022-45
- 60 TABLET in 1 BOTTLE (63187-022-60) · 63187-022-60
- 120 TABLET in 1 BOTTLE (63187-022-72) · 63187-022-72
- 90 TABLET in 1 BOTTLE (63187-022-90) · 63187-022-90
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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