United States · FDA National Drug Code directory
LEMTRADA
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
- 58468-0200_e9b870b2-1ea2-433f-991a-721c3cf582b1
- Product NDC
- 58468-0200
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- ALEMTUZUMAB
- Labeler
- Genzyme Corporation
- Marketing category
- BLA
- Marketing start / end (source format)
- 20141118
- Source listing expiry
- 20261231
Source-listed ingredients
- ALEMTUZUMAB — 12 mg/1.2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-USE in 1 CARTON (58468-0200-1) / 1.2 mL in 1 VIAL, SINGLE-USE · 58468-0200-1
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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