Product Details for: Rituxan
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
100MG/10ML (10MG/ML)
Single-Dose Vial
351(a)
Rituxan
Disc
002
Injection
Intravenous
500MG/50ML (10MG/ML)
Single-Dose Vial
351(a)
Rituxan
Disc
Proper Name
rituximab
rituximab
BLA Number
103737
103737
Applicant
IDEC Pharmaceuticals Corp.
IDEC Pharmaceuticals Corp.
Original Approval Date
February 19, 2002
February 19, 2002
Date of First Licensure