FDA Approval: ELIQUIS (APIXABAN) — Type 3 - New Dosage Form
Policy FDA-NDA220073 · Cardiology
HighEliquis (apixaban) has received approval for a new oral suspension dosage form under NDA220073, expanding access for patients unable to swallow tablets—likely pediatric or dysphagic populations. As an
View alertFDA Approval: ARGATROBAN IN SODIUM CHLORIDE (ARGATROBAN) — Type 5 - New Formulation or New Manufacturer
Policy FDA-NDA022434 · Cardiology
HighArgatroban in sodium chloride is an injectable medication that will likely receive a J-code for billing purposes under Medicare Part B. As an intravenous drug, it may also qualify for pass-through pay
View alertLCD L40255: Temporary Nontherapeutic Ambulatory Cardiac Monitoring Devices — Noridian
Policy LCD-L40255 (Notice Ends 06/20/2026) · Cardiology
HighThis final LCD from Noridian (JE/JF) governs coverage of temporary nontherapeutic ambulatory cardiac monitoring devices across 15 western states, effective June 21, 2026. It defines coverage criteria
View alertLCD L40257: Temporary Nontherapeutic Ambulatory Cardiac Monitoring Devices — Palmetto GBA
Policy LCD-L40257 (Notice Ends 06/27/2026) · Cardiology
HighPalmetto GBA has finalized LCD L40257 governing coverage of temporary nontherapeutic ambulatory cardiac monitoring devices across seven southeastern states, effective June 28, 2026. This LCD establish
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