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Purple Book
Database of Licensed Biological Products

Product Details for: Ocrevus Zunovo
Product Label Grayed out Product Label links indicate that there is no product label available for the product.

Product NumberDosage FormRoute of AdministrationStrengthProduct PresentationLicense TypeProprietary NameMarketing Status
001Injection Subcutaneous920MG/23ML; 23,000UNITS/23ML (40MG/1,000UNITS/ML)Single-Dose Vial351(a)Ocrevus ZunovoRx

Proper Name
ocrelizumab and hyaluronidase-ocsq

BLA Number
761371

Applicant
Genentech, Inc.

Original Approval Date
September 13, 2024

Date of First Licensure