Medical Injectable Drug Crysvita to Require Prior Authorization

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Medical Injectable Drug Crysvita to Require Prior Authorization

For: Professional and Facility Providers

Effective on the dates below, the medical injectable drug Crysvita will require prior authorization for all lines of business:

  • July 15, 2026 – Delaware, Pennsylvania, and West Virginia
  • Aug. 15, 2026 New York

Applicable Procedure Code Details

Procedure Code

Generic

Brand

J0584

burosumab-twza

Crysvita

Plan-preferred product and Site of Care considerations may apply in line with member benefits. Please confirm the most up-to-date coverage criteria outlined in Highmark’s applicable medical policies, which can be searched via the links available on the Medical Policies page of the Provider Resource Center (PRC).

Our List of Procedures and Durable Medical Equipment (DME) Requiring Authorization is subject to change. To view the current list for your region, go to the PRC's Obtaining Authorizations page.

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