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
- 41250-293_54f00ef3-e7e0-8c0a-e063-6294a90a5a3b
- Product NDC
- 41250-293
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Ibuprofen
- Labeler
- MEIJER DISTRIBUTION INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200319
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (41250-293-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE · 41250-293-15
- 1 BOTTLE in 1 CARTON (41250-293-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE · 41250-293-78
- 160 CAPSULE, LIQUID FILLED in 1 BOTTLE (41250-293-79) · 41250-293-79
- 300 CAPSULE, LIQUID FILLED in 1 BOTTLE (41250-293-83) · 41250-293-83
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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