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
- 41250-993_1335bd3f-e04d-4ea7-b2bf-975c2aaa2b11
- Product NDC
- 41250-993
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ibuprofen
- Labeler
- Meijer Distribution Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990301
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 225 TABLET, FILM COATED in 1 BOTTLE (41250-993-20) · 41250-993-20
- 100 TABLET, FILM COATED in 1 BOTTLE (41250-993-91) · 41250-993-91
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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