Product Details for: Zimrixby

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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(k) Biosimilar
Zimrixby
Rx
002
Injection
Intravenous
500MG/50ML (10MG/ML)
Single-Dose Vial
351(k) Biosimilar
Zimrixby
Rx
Proper Name
rituximab-cdxx
Reference Product Proper Name
rituximab
Reference Product Properietary Name
Rituxan
BLA Number
761376
Applicant
Dr. Reddy's Laboratories SA
Original Approval Date
July 31, 2026
Date of First Licensure
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