Product Details for: Ocrevus Zunovo Product Label Grayed out Product Label links indicate that there is no product label available for the product.
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 | Subcutaneous | 920MG/23ML; 23,000UNITS/23ML (40MG/1,000UNITS/ML) | Single-Dose Vial | 351(a) | Ocrevus Zunovo | Rx |
Proper Name
ocrelizumab and hyaluronidase-ocsq
BLA Number
761371
Applicant
Genentech, Inc.
Original Approval Date
September 13, 2024
Date of First Licensure