Code | Description | PA Coverage Criteria |
J9144 | INJECTION, DARATUMUMAB, 10MG AND HYALURONIDASE-FIHJ | Approval is determined by medical necessity criteria |
Q5108 | INJECTION, PEGFILGRASTIMJMDB, BIOSIMILAR, (FULPHILA), 0.5 MG | |
Q5110 | INJECTION, FILGRASTIM-AAFI, BIOSIMILAR, (NIVESTYM), 1 MCG | |
Q5111 | INJECTION, PEGFILGRASTIMCBQV, BIOSIMILAR, (UDENYCA), 0.5 MG | |
Q5101 | INJECTION, FILGRASTIM-SNDZ, BIOSIMILAR, (ZARXIO), 1 MCG | |
J1447 | INJECTION, TBO-FILGRASTIM, 1 MICROGRAM | |
J2506 | INJECTION, PEGFILGRASTIM, EXCLUDES BIOSIMILAR, 0.5 MG | |
J1442 | INJECTION, FILGRASTIM (G-CSF), EXCLUDES BIOSIMILARS, 1 MICROGRAM | Reserved for documentation of treatment failure of a 1st line short-acting G-CSF: filgrastim-sndz (Zarxio), tbo-filgrastim (Granix), or filgrastim-aafi (Nivestym). |
Q5120 | INJECTION, PEGFILGRASTIMBMEZ, BIOSIMILAR, (ZIEXTENZO), 0.5 MG | Reserved for documentation of treatment failure of a 1st line long-acting G-CSF: pegfilgrastim (Neulasta, Neulasta Onpro), pegfilgrastim-jmdb (Fulphila), or pegfilgrastimcbqv (Udenyca). |
Q5122 | INJECTION, PEGFILGRASTIMAPGF, BIOSIMILAR, (NYVEPRIA), 0.5 MG | |
J1756 | INJECTION, IRON SUCROSE, 1 MG | Reserved for patients with one or more of the following: a) Absolute iron deficiency anemia with a ferritin <30μg/L or TSAT <20% with treatment failure or inability to tolerate oral iron. b) Chronic kidney disease with or without dialysis with ferritin < 500μg/L and TSAT <30% with treatment failure or inability to tolerate oral iron for non-dialysis patients. c) Chemotherapy-induced anemia with ferritin 30-500μg/L or TSAT <50% in patients receiving ESAs. Ferritin must not exceed 800μg/L, and TSAT must not be ≥50%. Note: Code J1756 is limited to 1,200 mg per treatment cycle. |
Q0138 | INJECTION, FERUMOXYTOL, FOR TREATMENT OF IDA, 1 MG (NONESRD USE) | |
Q0139 | INJECTION, FERUMOXYTOL, FOR TREATMENT OF IDA, 1 MG (FOR ESRD ON DIALYSIS) | |
Q5105 | INJECTION, EPOETIN ALFA-EPBX, BIOSIMILAR, (RETACRIT) (FOR ESRD ON DIALYSIS), 100 UNITS | Reserved for patients who have Hemoglobin (Hgb) 20% or serum ferritin > 100 ng/ml at initiation. Hgb should be checked monthly and is not to exceed 11 g/dl. Authorization is for 12 months at a time. For renewal, Hgb must be below 11 g/dL. |
Q5106 | INJECTION, EPOETIN ALFA-EPBX, BIOSIMILAR, (RETACRIT) (FOR NON-ESRD USE), 1000 UNITS | |
J0885 | INJECTION, EPOETIN ALFA (FOR NON-ESRD USE), 1000 UNITS | Reserved for patients who have Hemoglobin (Hgb) 20% or serum ferritin > 100 ng/ml at initiation AND treatment failure or contraindication to Retacrit. Hgb should be checked monthly and is not to exceed 11 g/dl. When initiating therapy for anemia due to CKD, cumulative weekly dosing does not exceed the target range of 50 to 100 units/kg 3 times a week (300 units/kg weekly). Authorization is for 12 months at a time. For renewal, Hgb must be below 11 g/dL. |
Q4081 | INJECTION, EPOETIN ALFA, 100 UNITS (FOR ESRD ON DIALYSIS) |