Alert detail

FDA Approval: REVTORPYK (GEDATOLISIB) — Type 1 - New Molecular Entity

Policy ID: FDA-NDA219908Specialty: OncologyAdded: 7/18/2026Effective: 2026-07-14federal register
Routine

What changed

Revtorpyk (gedatolisib) approved; verify billing pathway vs. FDA label.

Who’s affected: Oncology billing teams · Effective: 2026-07-14

Primary source: View the official CMS/MAC document ↗

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