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
- 63629-1468_ffbc9f9d-60df-4552-80fa-e29c831ecc41
- Product NDC
- 63629-1468
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Bryant Ranch Prepack
- 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
- 20 TABLET in 1 BOTTLE (63629-1468-1) · 63629-1468-1
- 30 TABLET in 1 BOTTLE (63629-1468-2) · 63629-1468-2
- 40 TABLET in 1 BOTTLE (63629-1468-3) · 63629-1468-3
- 60 TABLET in 1 BOTTLE (63629-1468-4) · 63629-1468-4
- 90 TABLET in 1 BOTTLE (63629-1468-5) · 63629-1468-5
- 120 TABLET in 1 BOTTLE (63629-1468-6) · 63629-1468-6
- 100 TABLET in 1 BOTTLE (63629-1468-7) · 63629-1468-7
- 21 TABLET in 1 BOTTLE (63629-1468-8) · 63629-1468-8
- 15 TABLET in 1 BOTTLE (63629-1468-9) · 63629-1468-9
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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