06/16/2025 | Press release | Distributed by Public on 06/16/2025 09:04
TO: Pharmacies, Physicians, Physician Assistants, Nurse Practitioners, Oral Surgeons, Optometrists, Dentists, FQHCs, RHCs, Mental Health Service Providers and Nursing Homes
RE: Preferred Drug List (PDL) and Pharmacy Quarterly Update
Effective July 1, 2025, the Alabama Medicaid Agency (Medicaid) will:
1. Continue to monitor the stimulant shortage affecting ADHD medications. Should you need assistance, please contact Acentra Health at the number below for alternative prescribing and dispensing options.
2. Require PA for buprenorphine/naloxone sublingual film. Brand Suboxone will become non-preferred. Brand Zubsolv will also become non-preferred. Generic buprenorphine/naloxone sublingual tablets will remain preferred with clinical criteria. Please see below for additional information.
3. Require PA for generic dapagliflozin (generic Farxiga), generic dapagliflozin/metformin ER (generic Xigduo XR), generic lisdexamfetamine dimesylate capsules (generic Vyvanse capsules), generic rivaroxaban (generic Xarelto), and generic umeclidinium-vilanterol (generic Anoro Ellipta). Brands Farxiga, Xigduo XR, Vyvanse capsules, Xarelto, and Anoro Ellipta will be billed with a Dispense as Written (DAW) Code of 9. DAW Code of 9 indicates the following: Substitution Allowed by Prescriber but Plan Requests Brand. This value is used when the prescriber has indicated, in a manner specified by prevailing law, that generic substitution is permitted, but the Plan requests the brand product to be dispensed .
4. Update the PDL to reflect the quarterly updates listed below:
PDL Additions |
|
Brixadi CC |
Opiate Partial Agonists |
Fiasp |
Insulins |
Humalog |
Insulins |
infliximab (generic Remicade) CC |
Disease-Modifying Antirheumatic Agents |
methylphenidate ER (generic Concerta) |
Cerebral Stimulants/Agents for ADHD |
PDL Deletions |
|
AirDuo Respiclick |
Respiratory Corticosteroids |
buprenorphine/naloxone sublingual films |
Opiate Partial Agonists |
dapagliflozin (generic Farxiga) |
Sodium-glucose Co-transporter 2 Inhibitor |
dapagliflozin/metformin ER (generic Xigduo XR) |
Sodium-glucose Co-transporter 2 Inhibitor |
Invokamet |
Sodium-glucose Co-transporter 2 Inhibitor |
Invokana |
Sodium-glucose Co-transporter 2 Inhibitor |
lisdexamfetamine dimesylate capsules (generic Vyvanse capsules) |
Cerebral Stimulants/Agents for ADHD |
Novolog U-100 |
Insulins |
rivaroxaban (generic Xarelto) |
Oral Anticoagulants |
Suboxone |
Opiate Partial Agonists |
umeclidinium-vilanterol (generic Anoro Ellipta) |
Respiratory Beta-Adrenergic Agonists |
Zubsolv |
Opiate Partial Agonists |
CC This agent will be preferred with clinical criteria in place.
Medicaid Medications for Opioid Use Disorder (MOUD) Project - Program Update
Medicaid continues its commitment to improving access to evidence-based treatment for opioid use disorder (OUD) through the Medications for Opioid Use Disorder (MOUD) initiative. In January 2025, Medicaid launched Phase I of this multi-phase initiative, focused on expanding access and reducing administrative barriers to treatment.
Phase I Overview:
Phase I integrated opioid dependence medications into the Electronic Prior Authorization (EPA) program and streamlined access to preferred agents listed on the Agency's Preferred Drug List (PDL). A key enhancement involved automatic processing for buprenorphine-experienced recipients, defined as having at least one buprenorphine claim within the past 90 days. These subsequent fills are evaluated through the EPA system to confirm:
1. The recipient has a documented OUD diagnosis.
2. There is no record of opioid use within the preceding 30 days.
If both conditions are met, prior authorization is automatically approved at the pharmacy point-of-sale for up to a year's supply. If opioid use is detected in the past 30 days, a manual prior authorization (PA) request is required.
Phase II Overview:
Under Phase II, effective May 12, 2025, buprenorphine-naïve recipients, defined as those with no buprenorphine claims in the previous 90 days, may receive up to a 34-day supply of a preferred OUD medication at the pharmacy point-of-sale without requiring prior authorization. Claims for non-preferred buprenorphine products will be denied, and a manual PA must be submitted for consideration.
Effective July 1, 2025, the following are the preferred buprenorphine products:
Providers with questions regarding the MOUD program may contact the Alabama Medicaid Pharmacy Department at 334-242-5050.
For additional PDL and coverage information, visit our drug look-up site at
https://www.medicaid.alabamaservices.org/alportal/NDC%20Look%20Up/tabId/5/Default.aspx .
The PA request form and criteria booklet should be utilized by the prescriber or the dispensing pharmacy when requesting a PA. The PA request form can be completed and submitted electronically at https://medicaid.alabama.gov/content/9.0_Resources/9.4_Forms_Library/9.4.13_Pharmacy_Forms.aspx .
Providers requesting PAs by mail or fax should send requests to: