Product Details for: Campath

RETURN TO SEARCH RESULTS
PRODUCT LABEL Grayed out Product Label links indicate that there is no product label available for the product.
Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
30MG (10MG/ML)
Ampule
351(a)
Campath
Disc
002
Injection
Intravenous
12MG/1.2ML (10MG/ML)
Single-Dose Vial
351(a)
Lemtrada
Rx
003
Injection
Intravenous
30MG/1ML
Single-Dose Vial
351(a)
Campath
Rx
Proper Name
alemtuzumab
BLA Number
103948
Applicant
Genzyme Corporation
Original Approval Date
May 7, 2001
Date of First Licensure
RETURN TO SEARCH RESULTS