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
- 55910-399_e177a580-dbcd-6a37-e053-2995a90a6fb8
- Product NDC
- 55910-399
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Ibuprofen
- Labeler
- DOLGENCORP, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220712
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (55910-399-12) · 55910-399-12
- 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (55910-399-20) · 55910-399-20
- 1 BOTTLE in 1 CARTON (55910-399-23) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE · 55910-399-23
- 1 BOTTLE in 1 CARTON (55910-399-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE · 55910-399-80
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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