Medicaid Expansion Restricted Use Drug Precertification List
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List of prescription medications and medical-benefit drugs subject to precertification (prior authorization) and limited dispensing for Medicaid Expansion members; affects providers submitting medical or pharmacy benefit claims in North Dakota.
No material clinical or coverage changes in this revision.
Coverage Criteria
Precertification requirement
Covered when ALL of the following are met
Providers must use the medical drug prior authorization form for medical-benefit drugs (see provided link) and consult the Preferred Drug List (PDL) to determine pharmacy vs medical benefit processing.
Medications that are administered by the patient or another non‑professional and do not require professional administration are considered self‑administered and are not typically covered under the medical benefit. These items are generally processed through the pharmacy benefit per the Medical Policy: Medications and Diabetic Supplies Payable on the Pharmacy Benefit. Examples in this policy include continuous glucose monitor components (e.g., A9276 sensor, A9277 transmitter, A9278 receiver) and other codes noted as processed at pharmacy point‑of‑sale.
The lists of HCPCS/J/K/Q/S codes shown elsewhere in this document are a coding reference only and do not by themselves define clinical coverage or exclusions. Providers must use the applicable policy sections and medical necessity rules to determine coverage, and must submit prior authorization requests and claims using the correct HCPCS/J/K/Q/S codes shown in the coding tables.
Coding and Billing Codes
| Q2055 | ABECMA (idecabtagene vicleucel) |
| J0791 | ADAKVEO (crizanlizumab-tmca) |
| J9042 | ADCETRIS (brentuximab) |
| J0172 | ADUHELM (aducanumab-avwa) |
| J1931 | ALDURAZYME (laronidase) |
| J0256 | ARALAST NP / PROLASTIN-C / ZEMAIRA (alpha1-proteinase inhibitor) |
| J9302 | ARZERRA (ofatumumab) |
| J1554 | ASCENIV (immune globulin - IV) |
| J9118 | ASPARLAS (calaspargase pegol-mknl) |
| J9035 | AVASTIN (bevacizumab) / C9257 (oncology diagnosis only) |
| A9276 | Sensor; invasive, disposable, for use with interstitial CGM system, one unit = 1 day supply |
| A9277 | Transmitter; external, for use with interstitial CGM system |
| A9278 | Receiver (monitor); external, for use with interstitial CGM system |
| J0135 | Injection, adalimumab, 20 mg (Humira) |
| J0364 | Injection, apomorphine hydrochloride (Apokyn) |
| J0593 | Injection, lanadelumab-flyo, 1 mg (Takhzyro) |
| J0596 | Injection, C1 esterase inhibitor (recombinant), Ruconest, 10 units |
| J0597 | Injection, C-1 esterase inhibitor (human), Berinert, 10 units |
| J0598 | Injection, C-1 esterase inhibitor (human), Cinryze, 10 units |
| J0599 | Injection, C-1 esterase inhibitor (human), Haegarda, 10 units |
| J0597 | Injection, C-1 esterase inhibitor (human), Berinert, 10 units. |
| J0598 | Injection, C-1 esterase inhibitor (human), Cinryze, 10 units. |
| J0599 | Injection, c-1 esterase inhibitor (human), (Haegarda), 10 units. |
| J0717 | Injection, certolizumab pegol, 1 mg (Cimzia). |
| J1000 | Injection, depo-estradiol cypionate, up to 5 mg. |
| J1071 | Injection, testosterone cypionate, 1 mg. |
| J1110 | Injection, dihydroergotamine mesylate, per 1 mg (D.H.E. 45). |
| J1290 | Injection, ecallantide, 1 mg (Kalbitor). |
| J1438 | Injection, etanercept, 25 mg (Enbrel). |
| J1595 | Injection, glatiramer acetate, 20 mg (Copaxone). |
| J2212 | Injection, methylnaltrexone, 0.1 mg (Relistor). |
| J2793 | Injection, rilonacept, 1 mg (Arcalyst). |
| J2941 | Injection, somatropin, 1 mg (Genotropin, Humatrope, Norditropin, Nutropin AQ, Omnitrope, Saizen, Serostim, Zorbtive). |
| J3110 | Injection, teriparatide, 10 mcg (Forteo). |
| J3121 | Injection, testosterone enanthate, 1 mg. |
| J3145 | Injection, testosterone undecanoate, 1 mg (Aveed). |
| J3262 | Injection, tocilizumab, 1 mg (Actemra). |
| J3357 | Ustekinumab, for subcutaneous injection, 1 mg (Stelara). |
| J3535 | Drug administered through a metered dose inhaler. |
| J7170 | Injection, emicizumab-kxwh, 0.5 mg (Hemlibra). |
| J7175 | Injection, factor x, (human), 1 i.u. (Coagadex). |
| J7179 | Injection, von Willebrand factor (recombinant), (Vonvendi), 1 i.u. vwf:rco. |
| J7180 | Injection, factor XIII (antihemophilic factor, human), 1 i.u. (Corifact). |
| J7181 | Injection, factor XIII a-subunit, (recombinant), per IU (Tretten). |
| J7182 | Injection, factor VIII, (antihemophilic factor, recombinant), (Novoeight), per IU. |
| J7183 | Injection, von Willebrand factor complex (human), Wilate, 1 IU VWF:RCo. |
| J7185 | Injection, factor VIII (Antihemophilic factor, recombinant) (XYNTHA) per IU (Xyntha). |
| J7186 | Injection, antihemophilic factor VIII/von Willebrand factor complex (human), per factor VIII IU (Alphanate). |
| J7187 | Injection, von Willebrand factor complex (Humate-P), per IU VWF:RCo. |
| J7188 | Injection, factor VIII (antihemophilic factor, recombinant), (OBIZUR), per i.u. |
| J7192 | Factor VIII (antihemophilic factor, recombinant) per IU, not otherwise specified (Kogenate FS, Advate, Recombinate). |
| J7193 | Factor IX (antihemophilic factor, purified, non-recombinant) per IU (Alphanine SD, Mononine). |
| J7194 | Factor IX, complex, per IU (Profilnine). |
| J7195 | Injection, factor IX (antihemophilic factor, recombinant) per IU (Benefix, Ixinity). |
| J7198 | Anti-inhibitor, per IU (Feiba NF). |
| J7200 | Injection, factor IX, (antihemophilic factor, recombinant), Rixubis, per IU (Rixubis). |
| J7201 | Injection, factor ix, fc fusion protein, (recombinant), alprolix, 1 i.u. (Alprolix). |
| J7202 | Injection, factor ix, albumin fusion protein, (recombinant), idelvion, 1 i.u. (Idelvion). |
| J7203 | Injection, factor ix, (antihemophilic factor, recombinant) glycopegylated, (Rebinyn), 1 iu. |
| J7204 | Injection, factor viii, antihemophilic factor (recombinant), (Esperoct), glycopegylated-exei, per iu. |
| J7686 | Treprostinil, inhalation solution, FDA-approved final product, non-compounded, administered through DME, unit dose form 1.74 mg (Tyvaso). |
| K0553 | Supply allowance for therapeutic continuous glucose monitor (CGM), includes all supplies and accessories, 1 month supply = 1 unit of service. |
| K0554 | Receiver (monitor), dedicated, for use with therapeutic glucose continuous monitor system. |
| Q3027 | Injection, interferon beta-1a, 1 mcg for intramuscular use (Avonex). |
| Q3028 | Injection, interferon beta-1a, 1 mcg for subcutaneous use (Rebif). |
| Q4074 | Iloprost, inhalation solution, FDA-approved final product, non-compounded, administered through DME, unit dose form, up to 20 micrograms (Ventavis). |
| S0090 | Sildenafil citrate, 25 mg (Viagra). |
| S0117 | Tretinoin, topical 5 grams (Retin-A, Renova). |
| S0138 | Finasteride, 5 mg (Propecia, Proscar). |
| S1030 | Continuous noninvasive glucose monitoring device, purchase (for physician interpretation of date, use CPT code). |
Provider Actions and Requirements
Precertification / Prior Authorization required
Prior authorization (Precertification) is required for the listed restricted use drugs (both brand and generic equivalents) and for medical-benefit drugs administered using the specified HCPCS/J/Q codes; submit a precertification request and obtain approval before dispensing or administering these drugs when processed under the medical benefit.
- Both brand name drugs and generic equivalents require Precertification (Prior Approval).
- A precertification (prior authorization) request must be submitted and approved for the listed restricted use drug.
Precertification requires correct HCPCS code use
When requesting precertification or submitting claims, providers must use the appropriate HCPCS, J-, Q-, K-, and S- codes listed in this policy for the drug or supply being requested or billed.
Submit prior authorization with the appropriate HCPCS code
Submit prior authorization using the appropriate HCPCS code for the listed drug or supply when requesting precertification; the policy explicitly lists codes to be used for prior authorization and claim submission.
- The policy states prior authorization is required for drugs using specified HCPCS/J/Q codes and provides a comprehensive code list.
- Both brand and generic equivalents are subject to the same precertification requirements and coding expectations.
Use pharmacy point-of-sale processing for self‑administered supplies when applicable
When drugs or devices are processed through pharmacy point of sale (e.g., CGM supplies A9276–A9278 or other listed items), consult the PDL and use pharmacy billing processes rather than medical-benefit precertification forms.
- A9276–A9278 and other codes are processed through pharmacy point-of-sale systems according to the Department of Human Services.
- Consult the Preferred Drug List to confirm processing benefit and any additional prior authorization requirements.
Use medical prior authorization form and consult PDL
Providers must use the medical drug prior authorization (Precertification) form for drugs processed under the medical benefit; the fillable form is available at the URL provided in the policy.
- Medical drug prior authorization forms: https://www.bcbsnd.com/content/dam/bcbsnd/documents/forms/providers/precertification/outpatient-fillable.pdf
- Consult the Preferred Drug List (PDL) to determine whether a medication is processed through the pharmacy benefit or requires medical-benefit precertification.
Member services and grievance contacts
Direct members to Member Services for language assistance, accessibility support, or to obtain grievance forms; providers may advise members to contact Member Services or the Civil Rights Coordinator for help filing grievances.
- Member Services phone (toll-free): 1-833-777-5779 (TTY: 1-800-366-6888 or 711).
- Grievance forms and filing instructions are available at www.medicaid.bcbsnd.com; Civil Rights Coordinator contact details are listed in the policy.
Precertification required — risk of denial/non-payment
Failure to obtain precertification (prior approval) for listed restricted-use drugs when required may result in denial of coverage or non-payment for the drug when it is subject to the medical benefit or limited dispensing.
- Obtain and document prior authorization approval before administering or billing medical-benefit restricted drugs to avoid claim denials or non-payment.
Coding-based denial risk — use listed HCPCS/J/K/Q/S codes
Claims and precertification requests must include the specific HCPCS/J/K/Q/S code that corresponds to the drug or supply; omission or incorrect coding can cause precertification or claim processing issues and potential denials.
Site of Care / Benefit Processing
Determine site of care and billing based on benefit and administration
Medications that do not require professional administration are considered self‑administered and are typically processed on the pharmacy benefit; determine site-of-care and billing path (office/infusion center vs pharmacy) based on benefit and administration.
- Self‑administered items (e.g., CGM sensors/transmitters/receivers, certain injectable drugs when self-administered) are processed via pharmacy point-of-sale systems per the policy.
- Medical‑benefit administration requires appropriate facility/provider coding (office or infusion center) and precertification when applicable.
Definitions
Background
This policy enumerates medications, biologics, and associated billing codes that require precertification (prior authorization) for Medicaid Expansion members in North Dakota. Both brand and generic equivalents listed require precertification when billed under the medical benefit or when the code is included on this restricted‑use list. Providers must submit and obtain an approved precertification before the drug or medical‑benefit administration to avoid potential denial of coverage or non‑payment.
Precertification applies to medications billed with the HCPCS/J/Q/K/S codes listed in the coding sections (including specialty biologics, immune globulins, CAR‑T and gene therapies, hemostasis factors, inhalation products, device supplies and smoking cessation S‑codes). For items that do not require professional administration and are processed at point of sale (for example certain CGM components coded A9276, A9277, A9278), processing may occur via the pharmacy benefit and providers should consult the Preferred Drug List and the Medical Policy on pharmacy‑payable supplies to determine the appropriate benefit and submission process.
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