LEMTRADA
Active substance: alemtuzumab
INJECTION, SOLUTION, CONCENTRATE · ALEMTUZUMAB 12 mg/1.2mL
United StatesActive
Marketing holder: Genzyme Corporation
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 3
Composition
- ALEMTUZUMAB · 12 mg/1.2mL
Analogues by country
Products with the same active substance registered in other countries.
| Country | Products |
|---|---|
| RU 4 |
|
| EU 2 |
|
Import and control
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c3-2fa0-7120-be30-690aea2b300e,01a120c3-5e76-71f3-a556-d83ccc42e748,01a120c5-544f-72ce-b127-ec976e08bdc6,01a120c5-924c-7782-a32c-5cc87c4351d3;count=4 · valid from 2026-10-09 · verified 2026-10-09
- United Statesprescription only
Source: openFDA NDC · record 01a12096-6195-729b-a6cc-7352d5acdb16,01a1209b-4fbb-7a16-a386-9eb5596a1387;count=2 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 58468-0200
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAVENOUS
Sources
- product · openFDA NDC · 58468-0200 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 58468-0200 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 58468-0200 · Verified 2026-10-09 · open in source