50242-554 : Ocrevus Zunovo Subcutaneous Injection, Solution


NDC: 50242-554
Labeler: Genentech, Inc.
Product Type: Human Prescription Drug
Drug Name:  Ocrevus Zunovo
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA761371
Rev. Date: 


NDC Package Codes:

  • 50242-554-01: 1 VIAL, SINGLE‑USE IN 1 CARTON (50242‑554‑01) / 23 ML IN 1 VIAL, SINGLE‑USE
  • 50242-554-86: 1 VIAL, SINGLE‑USE IN 1 CARTON (50242‑554‑86) / 23 ML IN 1 VIAL, SINGLE‑USE

Active Ingredients:

  • Hyaluronidase (Human Recombinant)
  • Ocrelizumab

Dosage Strength:

  • 23000 U/23mL
  • 920 mg/23mL

Pharmaceutical Classes:

  • Antibodies
  • Monoclonal [CS]
  • Antibodies
  • Monoclonal
  • Humanized [CS]
  • CD20-directed Antibody Interactions [MoA]
  • CD20-directed Cytolytic Antibody [EPC]
  • Endoglycosidase [EPC]
  • Glycoside Hydrolases [CS]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.