Medicaid-Approved Preferred Drug List (PDL)
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A Medicaid Preferred Drug List governing coverage, prior authorization, quantity limits, specialty pharmacy and step therapy indicators for outpatient prescription drugs for members covered by Empire BlueCross Medicaid in North Carolina.
No material clinical or coverage changes in this revision.
Coverage Criteria and Legend
Coverage flags and routing
Coverage and routing are determined by plan note flags assigned to each drug entry. When a product line includes one or more of the annotations below, the corresponding administrative action or routing applies.
This segment lists which drugs have these flags but does not include the full clinical criteria for approvals; follow payer processes for PA and SP routing.
Submit supporting clinical documentation as required by the payer when requesting PA.
Failure to route SP products through the specialty channel may cause denial or processing delays.
Numeric limits are product-specific and defined elsewhere; provide dosing and duration justification when requesting overrides.
Age documentation should be included when required.
Follow dispense/designation instructions and any preferred-product edits during adjudication.
This section functions as a formulary legend: individual drug and formulation lines are listed alphabetically with plan note annotations that govern coverage and routing. Common annotations shown include PA (prior authorization), QL (quantity limit), OTC (over‑the‑counter) and other operational notes; coverage and authorization for a listed product is determined by the specific note(s) appearing next to that formulation.
No explicit clinical exclusion language appears in this fragment. Entries are limited to product names, formulations and short plan notes (e.g., PA, QL, OTC) that indicate utilization controls rather than full clinical exclusion criteria.
This excerpt does not contain detailed medical‑necessity criteria or the full authorization requirements for products annotated with utilization flags. The legend identifies which products carry flags (for example, PA or QL) but does not include the underlying clinical approval criteria.
Within this legend excerpt there are no explicit exclusions stated. Items are annotated with operational notes such as OTC, QL or PA, but the excerpt does not include statements designating any product as excluded from coverage.
No explicit exclusions are provided in this segment of the legend. Lines for supplies, devices and medications are annotated with payer notes (for example, OTC, QL, PA) but exclusionary language is not present in these chunks.
The excerpt is primarily a listing of products and formulations with short annotations. It does not present full coverage criteria or step‑by‑step medical necessity rules for the listed medications; instead it flags products that require further administrivia (e.g., PA) or that are subject to limits (QL).
This portion of the document is a legend‑only section: individual product lines are shown with plan notes (OTC, QL, PA, etc.). The listing style is product‑centric and does not contain the complete coverage criteria or approval workflows for those annotations.
The content here serves as a legend—items are identified and may carry notes such as PA, QL or AL. The legend itself does not include the step‑by‑step authorization instructions; individual entries may direct providers to seek further detail where a plan note is present.
This segment does not explicitly list any products as not medically necessary. The excerpt is informational and limited to product lines and their short plan notes rather than clinical determinations of non‑coverage.
Formulary Listings and Code Tables
| OZEMPIC (0.25 OR 0.5 MG/DOSE) | Subcutaneous solution pen-injector — Notes = PA; QL |
| OZEMPIC (1 MG/DOSE) | Subcutaneous solution pen-injector — Notes = PA; QL |
| OZEMPIC (2 MG/DOSE) | Subcutaneous solution pen-injector — Notes = PA; QL |
| JANUMET ORAL TABLET | Notes = PA; QL |
| JANUMET XR ORAL TABLET EXTENDED RELEASE 24 HOUR | Notes = PA; QL |
| JANUVIA ORAL TABLET | Notes = PA; QL |
| liraglutide subcutaneous solution pen-injector | Reference = Victoza — Notes = PA; QL |
| escitalopram oxalate oral tablet | Reference = Lexapro |
| sertraline hcl oral tablet | Reference = Zoloft |
| venlafaxine hcl er oral capsule extended release 24 hour | Reference = Effexor XR — Notes = QL |
| NDC not provided | Document lists drug products and formulations but does not provide NDC values in this segment. |
Provider Actions, Prior Authorization & Documentation
Prior Authorization Required
Prior authorization is required for any product annotated with PA in the formulary. Providers must obtain prior authorization before dispensing or billing PA‑designated medications or supplies; failure to secure PA may result in claim denial or noncoverage.
- Obtain PA prior to dispensing when the Notes field includes PA.
- Claims for PA items must include the authorization number or supporting documentation per Empire BlueCross processes.
PA Examples & Scope
Many high‑cost, specialty, and select products are marked PA, sometimes together with SP (specialty pharmacy) and/or QL (quantity limits). Examples include specialty biologics, injectable therapies, select oral agents, CGM devices and sensors, insulin delivery supplies, migraine biologics, and certain ophthalmic and nasal agents — these require PA and/or specialty routing as noted.
- Examples of PA‑marked prescription drugs and biologics: dapagliflozin‑containing agents, OZEMPIC, JANUMET, JANUVIA, liraglutide, DUPIXENT, REPATHA, ALYQ, ambrisentan, sildenafil (Revatio), tadalafil (PAH).
- Examples of PA‑marked specialty/high‑cost injectables: many biologics (e.g., DUPIXENT, XOLAIR, ARANESP, MVASI) and HAE therapies (HAEGARDA, TAKHZYRO, RUCONEST).
- Examples of PA‑marked migraine and neurology products: AIMOVIG, EMGALITY, NURTEC, various triptans when noted PA.
- Examples of PA‑marked ophthalmic and ENT agents: cyclosporine ophthalmic (Restasis), LASTACAFT, select ophthalmic anti‑infectives; selected nasal sprays such as FLONASE formulations annotated PA.
Prior Authorization for CGM Devices & Diabetes Supplies
Continuous glucose monitoring (CGM) systems and many diabetes supplies listed with PA require prior authorization and clinical justification. Examples include Dexcom G6/G7 receivers, sensors and transmitters; FreeStyle Libre readers and sensors; Omnipod starter kits and pods; and certain meter kits, insulin syringes and pen needles annotated PA.
- CGM devices/sensors noted PA: DEXCOM G6 receiver/sensor/transmitter; DEXCOM G7 receiver/sensor; FREESTYLE LIBRE 2/3 sensors and readers.
- Insulin delivery and supply examples: OMNIPOD kits/pods (PA; QL), meter kits annotated PA; insulin syringes and many pen needles annotated PA.
- Documentation should include patient diagnosis, prior therapies, and rationale for device selection.
Utilization Management & Denial Risk
Utilization management flags (PA, QL, SP, AL, DO, ST) are operational controls that can trigger claim denials or require specific routing. Review Notes on each product and follow the payer’s PA and specialty pharmacy routing instructions.
- PA: prior authorization required; obtain approval before dispensing.
- QL: quantity limits — requests exceeding QL require justification.
- SP: specialty pharmacy — product may need to be dispensed via a specialty channel; claims filled outside required channel risk denial.
- AL/DO/ST: age limits, dose optimization, or step therapy requirements noted in class entries must be followed when present.
Documentation Expectations & Submission
Documentation must accompany PA requests and claims for PA and SP items. Submit clinical justification, prior therapy history (when applicable), and any age/quantity evidence needed to support medical necessity. Quantity limit overrides require supporting documentation explaining need for quantities above the QL.
- When PA is indicated submit supporting clinical records, previous medication trials, and treatment rationale.
- For SP items include specialty‑pharmacy routing details and any required enrollment documentation.
- For AL/QL items document patient age and clinical reason when prescribing outside standard age/quantity limits.
Prior Authorization and Quantity Limits for Opioids
Controlled substances and opioid formulations frequently carry both PA and QL annotations. Providers must follow opioid PA processes and document prior treatments and justification to support medical necessity.
- Many opioid products (e.g., morphine ER, oxycodone formulations, tramadol combinations) are annotated PA; follow opioid prior authorization rules.
- Requests exceeding QL for controlled analgesics require clinical rationale and supporting records to reduce denial risk.
Formulary Preference, Step Edits & Specialty Program Notes
Formulary preference notes (DO), step edits (ST), and specialty program indicators (SP) affect prior authorization and dispensing. Where step therapy or preferred‑product guidance exists, document attempted or contraindicated therapies if requesting non‑preferred products.
- DO: dose optimization or preferred dosing guidance — follow when applicable.
- ST: step therapy may require trial of preferred agents prior to authorization of non‑preferred drugs; document trials or contraindications.
- SP: specialty program requirements may mandate use of designated specialty pharmacy and adherence to program enrollment.
OTC Prescription Note
OTC products listed with the OTC note may be covered only when prescribed; prescribers should indicate OTC on the prescription when coverage is sought. Some OTC items still carry QL or PA annotations — confirm Notes.
- When dispensing OTC medications via prescription, prescribers MUST indicate "OTC" on the prescription per payer instruction.
- OTC status does not remove PA or QL requirements if those flags are present for the specific item.
Key Abbreviations and Definitions
Step Therapy Indicators and Notes
| Reference | Summary |
|---|---|
| inv-131 | |
| ST flag indicates step therapy is required for some agents; specific step sequences are not listed in this legend excerpt. |
| Reference | Summary |
|---|---|
| inv-132 | |
| Entries annotated with DO may indicate formulary-preferred products or dose/dispense edits and could be used to implement step edits or preferred-agent requirements. |
| Reference | Summary |
|---|---|
| inv-133 | |
| Some antidiabetic agents and GLP-1 agonists (examples: dapagliflozin-containing products, OZEMPIC, liraglutide) are marked PA and may be subject to step edits elsewhere in the policy. |
| Reference | Summary |
|---|---|
| inv-134 | |
| Long-acting injectable antipsychotics and some specialty psychotropics are annotated with PA and AL/QL which may imply administrative step or monitoring requirements prior to approval. |
| Reference | Summary |
|---|---|
| inv-135 | |
| Some products include DO and AL annotations suggesting dispensing or step requirements; explicit step-therapy sequences are not provided in this excerpt. |
| Reference | Summary |
|---|---|
| inv-136 | |
| Step therapy is required for specific pulmonary arterial hypertension agents and select branded products (entries marked PA; SP; QL indicate step/authorization expectations). |
| Reference | Summary |
|---|---|
| inv-137 | |
| No explicit step therapy rules are listed in this segment; only annotations such as PA, QL, SP are present in the legend portion. |
| Reference | Summary |
|---|---|
| inv-138 | |
| No explicit step therapy entries appear in this excerpt; the legend provides annotations but does not define step logic here. |
| Reference | Summary |
|---|---|
| inv-139 | |
| This legend portion does not list step therapy requirements; entries are annotated (PA, QL, OTC) but no step sequences are specified. |
| Reference | Summary |
|---|---|
| inv-140 | |
| No explicit step therapy steps specified in this excerpt; some items are flagged SP (specialty) indicating special handling rather than defined step sequences. |
| Reference | Summary |
|---|---|
| inv-141 | |
| No explicit step-therapy sequences listed in these chunks; riluzole and other entries are noted PA; SP which may imply specialty handling rather than formal step requirements in this legend. |
| Reference | Summary |
|---|---|
| inv-142 | |
| Some specialty agents are annotated 'PA; SP; QL' which implies specialty pharmacy dispensing and prior authorization steps are required for coverage though detailed step sequences are not provided here. |
| Reference | Summary |
|---|---|
| inv-143 | |
| No step therapy is specified in this legend portion; if step rules exist they are defined elsewhere in the policy document rather than in this excerpt. |
Quantity Limits (QL) Notes
Site of Care and Specialty Administration
Background and Scope
This document is a Medicaid Preferred Drug List organized by therapeutic class and alphabetized within class. It displays individual products and formulations with plan flags (for example, PA, QL, OTC, SP, AL, DO) that indicate prior authorization, quantity limits, specialty pharmacy routing, age limits or dispense instructions which determine coverage processing and provider actions.
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