01Effective November 1, 2026.
02Billing team should review all active prescriptions and pending claims for the affected drug classes to identify which patients are receiving drugs that changed status on the PDL.
03For drugs moved to preferred with prior authorization (Macitentan, Ambrisentan, Tofacitinib IR/ER tablets, Fulphila), get prior authorization before processing claims; claims without prior auth will be denied.
04For drugs moved to non-preferred (Tofacitinib solution, Xeljanz IR tablet and solution, Milnacipran, Drizalma sprinkle capsule, Gabapentin ER, Filkri, Fylnetra, Nypozi, Rolvedon, Ryzneuta, Stimufend, Timolol generic, Zolymbus gel), inform providers that these now require prior authorization or will have reduced coverage; coordinate with prescribers and pharmacies on coverage options.
05For drugs removed from the PDL (Adcirca, Idacio, Cymbalta, Basaglar TempoPen, insulin degludec generic, Phospholine iodide, Betoptic, Betoptic S, Betagan, Ocupress, Timoptic, Timoptic-XE, Trusopt, Xelpros, Vascepa, Lovaza), stop billing these drugs for Nevada Medicaid patients; communicate with prescribers and front desk staff that alternatives must be selected and that patients who still request discontinued drugs should understand they may not be covered.
06Update charge entry and claim submission edits to route affected medications to the correct prior authorization workflow and to flag non-preferred drugs before claims are submitted.
07Watch for member denials and appeals related to prior authorization lapses or non-preferred drug usage, and resubmit claims with proper prior authorization documentation when available.