2025 Drug List (Pharmacy formulary) — Coverage Criteria
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A formulary drug list that describes covered outpatient prescription drugs, tiers, special requirements, and coverage processes for Blue Cross Blue Shield of Oklahoma members and their providers.
No material clinical or coverage changes in this revision.
Coverage Criteria and Formulary Rules
Formulary inclusion
Covered when ALL of the following are met
Members and prescribers should consult the most current Drug List at MyPrime.com or bcbsok.com for updates.
Utilization management requirements
Coverage may be conditional on utilization management requirements
Special Requirements flags appear next to medications on the Drug List.
Coverage stance by drug entry
Coverage status is implicit per drug line as Tier, and Requirements/Limits indicating PA, QL, and SP where applicable.
Specific clinical eligibility criteria for PA (e.g., diagnosis codes, prior therapy) are not provided within these drug-line chunks and must be obtained via the PA process when applicable.
Formulary coverage flags (by drug)
Drugs are listed with their formulary tier and any Requirements/Limits; coverage is governed by those flags (PA, QL, SP).
See the Drug List entries for the exact Requirements/Limits per product (examples include TRIKAFTA PA, QL (56 packets/28 days), SP; ZYMFENTRA PA, QL (2 kits/28 days), SP).
Formulary entries (coverage with utilization controls)
Coverage entries are product-level with associated controls; listed as Covered with utilization controls where applicable.
Examples in the Drug List include starter/titration packs (MAYZENT STARTER PACK Requirements/Limits = PA, QL (7 tablets/180 days), SP) and therapy packs with QL/PA noted (e.g., MAVENCLAD therapy packs).
Drugs that are not shown on the BCBSOK Drug List are not covered. The formulary is updated regularly and coverage decisions reflect FDA approval, safety, efficacy, and comparative reviews by a clinical committee; for current listings consult MyPrime.com or the BCBSOK provider portal. Certain product categories may be expressly excluded by plan materials (examples noted include some over‑the‑counter equivalents, repackaged medications, compounded preparations, and non‑FDA‑approved drugs).
When a product entry shows Special Requirements (for example PA, QL, SP, ST, or AC), those utilization management controls must be met for coverage — see the product line for the specific flags and limits.
The vaccine product VIVOTIF (typhoid vaccine, delayed‑release capsule) is listed with a Drug Tier = NP and no Requirements/Limits recorded in this excerpt. The presence of a nonpreferred tier does not itself state an exclusion; check the full drug list and the member’s plan materials for any plan‑specific coverage or utilization controls.
The provided formulary excerpts do not include explicit clinical exclusion criteria tied to the listed specialty products; entries instead show Drug Tier and Requirements/Limits (for example, many specialty agents are marked SP or PA). Where clinical eligibility criteria for prior authorization exist, those criteria are documented in the payer’s authorization processes rather than on the line‑item excerpts shown here.
Within the chunks shown there are no explicit coverage exclusions described for the product groups; the entries report Drug Tier and any Special Requirements (e.g., PA, QL, SP) that govern access. For plan‑specific exclusions, refer to the member’s benefit materials.
These drug‑line extracts do not state explicit product exclusions. Coverage is presented at the product level with tier assignments and utilization flags; absence of an exclusion statement in these chunks does not imply unrestricted coverage — applicable limits or prior authorization requirements shown on the line must be met.
No explicit exclusions for specific products are listed in the referenced chunk. Entries for titration packs, nicotine replacement products, and memantine formulations show tiers and Requirement/Limits codes (for example AC or QL) but do not include line‑level exclusion language in this excerpt.
Medications used off‑label beyond FDA‑approved labeling or not supported by recognized evidence‑based clinical practice guidelines may be limited to FDA‑approved indications per the plan. Coverage decisions consider FDA labeling and recognized guidelines; where off‑label use is requested, documentation supporting medical necessity consistent with plan rules will be required.
In the provided excerpts there are no explicit statements labeling therapies as not medically necessary. The document instead records product tiers and utilization controls; any determinations of not medically necessary would be made through the payer’s coverage review and exception processes as reflected in plan materials.
These chunks do not contain explicit 'not medically necessary' (NMN) declarations. Coverage stance for products is communicated via Drug Tier and Requirements/Limits (e.g., PA, QL, SP); NMN determinations, when applicable, are handled through prior authorization and exception review processes described elsewhere in plan documentation.
This portion of the formulary does not include explicit 'not medically necessary' language. Product entries list tiers and special requirements (for example, QL and ST) that define access controls rather than blanket NMN statements.
Codes, Supply Durations, and Program Flags
| N/A | Drug list entries (no billing or procedure codes present in this section) |
| No codes listed |
| NDC-like / presentation text | Vaccine and biologic product presentations as listed (e.g., FLUAD 2025-2026 influenza vac pref syr 0.5 ml); exact billing codes not provided in the excerpt. |
| PALFORZIA_LEVEL_X | Palforzia product level entries (Initial Dose, Level 0-11) with specified mg doses; Requirements/Limits = SP. |
| drug_strength_entries | Antineoplastic and targeted therapy drug entries with strengths (e.g., abiraterone acetate 250 mg, 500 mg; IBRANCE palbociclib 75/100/125 mg). No CPT/HCPCS/ICD codes provided. |
| AC | Access control / administrative requirement |
| PA | Prior authorization required |
| QL | Quantity limit (amount/unit specified alongside drug) |
| SP | Step therapy / specialty program flag |
| N/A | This section lists NDCs and formulary entries but no procedure/diagnosis codes in these chunks. |
| N/A | This portion contains drug names, tiers, and requirements but no procedure/CPT/HCPCS/ICD-10/NDC codes in these chunks. |
| No codes listed |
Prior Authorization, Step Therapy, Documentation, and Denial Risk
Prior Authorization Required
Prior Authorization (PA) is required for many medications listed in this document. When a PA is indicated, the prescriber must submit and receive approval before the drug will be covered. Items marked with “PA” or shown with PA/SP/QL flags in the formulary may be denied at point-of-sale or returned if authorization is not obtained.
- Obtain PA prior to dispensing for drugs noted with PA or PA, SP flags (e.g., many specialty and oncology agents).
- PA denials: BCBSOK will notify the prescriber and offer a covered alternative when applicable.
Prior Authorization for Select Antivirals
Several high-cost antivirals and hepatitis C agents require prior authorization and often have additional program flags (SP, QL). Examples include MAVYRET, VOSEVI, SOVALDI, HARVONI, and other direct-acting antivirals — claims may deny without PA.
- Commonly PA-required antivirals: MAVYRET, VOSEVI, SOVALDI, HARVONI.
- Expect quantity limits (QL) and specialty program (SP) flags alongside PA for these agents.
Administrative Coverage (AC) for Vaccines
Some vaccines and certain administration products are flagged with an Administrative Coverage (AC) requirement. Confirm appropriate administration and billing codes before submission to ensure coverage.
- Vaccines commonly marked AC include seasonal influenza products, COVID-19 vaccine formulations, HPV (GARDASIL 9), and pediatric conjugate vaccines.
- Verify CPT/administration coding and member eligibility prior to billing.
PA for Select Antidiabetic / Weight-Management Products
Select antidiabetic and weight-management agents require prior authorization and may have QL/SP constraints. Examples include MOUNJARO, OZEMPIC, RYBELSUS, SAXENDA, WEGOVY and similar GLP-1 or dual-agonist products.
- PA is required before coverage for many GLP-1 and weight-management agents.
- Quantity limits (pens/doses per days supply) and specialty program flags commonly apply.
Prior Authorization for Many Specialty and Oncology Agents
Many specialty, biologic, and oncology agents require prior authorization and are often subject to quantity limits and specialty program management. Examples include TALZENNA, REPATHA, OMNITROPE, SKYTROFA, NUCALA, FASENRA, TEZSPIRE, TRIKAFTA and numerous oncology therapies.
- Obtain PA for listed specialty and oncology drugs prior to dispensing to avoid denial.
- Specialty program (SP) and quantity limits (QL) are frequently applied and must be documented.
Prior Authorization and Exception Submissions; Documentation Required
Prior authorization requests and exception submissions must include adequate supporting documentation of medical necessity. Providers should use the contact information on the member ID card to initiate PA or exception requests and may request expedited review when the condition is urgent.
- Include diagnosis, prior medication trials (when applicable), relevant labs or imaging, and intended quantity/days' supply when submitting PA.
- Expedited review available for conditions that jeopardize life, health, or function (72-hour decision timeframe).
Formulary Requirement Fields and How to Interpret Flags
Formulary requirement fields include flags such as PA (Prior Authorization), QL (Quantity Limits), SP (Specialty Program), AC (Administrative Coverage), and ST (Step Therapy). These indicators signal additional actions required by the provider or risks at point-of-sale.
- PA = prior authorization required; QL = quantity or dispensing limit; SP = specialty program; AC = administrative coverage (often vaccines/administration); ST = step therapy required.
- Failure to adhere to flagged requirements may result in claim denial or non-covered dispensing.
Quantity Limit and Step Therapy Documentation
Quantity limits (QL) and step therapy (ST) requirements commonly accompany PA. When requesting PA or exceptions, include documentation to support requests to exceed QL or to bypass ST (prior trials, rationale, and clinical records).
- Document prior medication trials, clinical rationale to exceed QL, and the specific days' supply requested.
- When step therapy applies, include evidence of intolerance or failure of required prior agents to request exception.
Step Therapy — When It Applies and When Details May Be Absent
Step therapy (ST) is applied to selected agents across multiple classes (e.g., certain CNS/antipsychotic agents, migraine, and others). Some entries in this segment do not specify a step sequence — review plan materials for exact ST requirements.
- If ST is indicated (ST flag), providers must document that required prior agents were tried and failed or were not tolerated before PA will be approved.
- When step details are not specified in the formulary document, use the member’s benefit plan materials or PA criteria to determine required prior steps.
Denial Risk and Consequences
Failure to obtain required prior authorization or to adhere to quantity limits/step therapy may result in denial or a requirement to pay the full cost of the medication. BCBSOK will notify the prescriber and (when applicable) offer a covered alternative if a PA or exception is denied.
- Claims presented without required PA may be denied at point-of-sale.
- If dispensed in excess of QL (including certain controlled substances), state law or plan rules may prevent coverage and member may be responsible for full cost.
Initial Coverage and Initiation Controls
Initial coverage by drug line
Formulary entries include tiering and utilization controls that guide initial access
No additional diagnosis-specific initiation criteria are included in these chunks; providers should follow PA documentation requirements when submitting initial authorization requests.
Initiation flags
Formulary flags for initiating therapy
Examples: CREON and ZENPEP are listed with tier and may have Requirements/Limits; specific PA clinical criteria are managed through the PA process.
Starter/titration pack controls
Starter packs and titration packs are listed with QL and PA controls
Example entries: MAYZENT STARTER PACK Requirements/Limits = PA, QL (7 tablets/180 days), SP; LUMRYZ STARTER PACK Requirements/Limits = QL (28 packets/180 days), SP PA.
Step Therapy Rules and Affected Products
| Summary | Source detail |
|---|---|
| Step therapy (ST) may require trial of a proven, cost‑effective medication before coverage of the requested drug is available. | |
| Document: 'Step Therapy (ST): Your benefit plan may include a step therapy program... if a step therapy is commonly required, it will generally be noted next to the medication with an "ST" under the Special Requirements column.' |
| Observation | Example entries / flags |
|---|---|
| Several hepatitis C and other antiviral agents are managed with prior authorization and specialty designations; explicit step sequences are not provided in the drug list excerpt. | |
| Example: MAVYRET marked 'PA, QL (90 tablets/30 days), SP' (MAVYRET shown with PA/SP flags). Document notes explicit step sequences are not present in these chunks. |
| Observation | Example entries / flags |
|---|---|
| Many oncology and antineoplastic products carry utilization controls (PA, QL, SP) but the document does not list multi‑step therapy sequences in the excerpt. | |
| Examples: abiraterone acetate listed with 'PA, QL (60 tablets/30 days), SP'; multiple oncology agents show PA/QL and SP designations without step sequences. |
| Observation | Example entries / flags |
|---|---|
| Contraceptive products frequently include administrative coverage (AC) and quantity limits; some entries also show PA — these flags imply formulary management though explicit step therapy rules are not provided. | |
| Examples: multiple oral contraceptives and patches listed with 'AC' and 'QL (28 tablets/21 days)'; some entries include 'AC, PA, QL' (e.g., ELLA listed with AC, QL (2 tablets/365 days), and some products show AC, PA, QL). |
| Observation | Example entries / flags |
|---|---|
| Certain agents are designated 'SP' or managed via a step/specialty program; the presence of 'SP' indicates specialty program handling that may include step components. | |
| Examples: MIGLITOL and MOUNJARO entries list 'PA, QL, SP' indicating specialty program/step program flags (MOUNJARO shows PA, QL, SP in the Requirements/Limits). |
| Observation | Example entries / flags |
|---|---|
| Step program / specialty program (SP) designations appear for select agents; these entries typically also carry PA and QL constraints, but the document does not specify full step sequences. | |
| Examples: MOUNJARO listed with 'PA, QL, SP'; Palforzia product levels are listed with 'SP' indicating specialty program handling without explicit step sequencing in the excerpt. |
| Observation | Example entries / flags |
|---|---|
| Several products are designated NP (nonpreferred) and/or require prior authorization; explicit multi‑step sequences are not shown in these chunks. | |
| Examples: NULIBRY and OCTREOTIDE entries show 'SP' (specialty) and OMNITROPE shows 'PA, SP'; NEXLETOL listed with 'PA, QL (30 tablets/30 days)'. |
| Observation | Example entries / flags |
|---|---|
| Specialty pharmacy (SP) designations are used for many biologic and specialty agents; these entries commonly include PA and QL as utilization controls rather than detailed step therapy sequences. | |
| Examples: BYLVAY listed with 'PA, SP'; CIMZIA shows 'PA, QL (2 kits/28 days), SP'; OMVOH listed with 'PA, QL (2 pens/28 days), SP'. |
| Observation | Example entries / flags |
|---|---|
| The document applies utilization management primarily via prior authorization (PA) and quantity limits (QL); explicit step therapy sequences are not provided in these sections. | |
| Examples: inhaler and nebulizer products show QL limits (e.g., ADVAIR HFA QL inhaler/30 days); NUCALA shows 'PA, QL (3 ml/28 days), SP' — controls are applied without step sequences listed. |
| Observation | Example entries / flags |
|---|---|
| Biologics and other specialty agents are frequently subject to specialty program or step designations (SP) and prior authorization; specific step requirements are not enumerated in the excerpt. | |
| Examples: CIMZIA, OMVOH, and other biologics show 'PA' and 'SP' with QL limits (e.g., CIMZIA 'PA, QL (2 kits/28 days), SP'). |
| Observation | Example entries / flags |
|---|---|
| Step therapy (ST) is explicitly applied to certain CNS and antidepressant agents in the list; products marked 'ST' require a step‑therapy trial prior to coverage as noted. | |
| Examples: FETZIMA (levomilnacipran) therapy pack and other antidepressant therapy packs show 'QL (150 tablets/30 days) = ST'; aripiprazole formulations and clozapine entries include 'ST' alongside QL limits (aripiprazole entries show 'QL... , ST'). |
| Observation | Source detail / examples |
|---|---|
| Products flagged with 'ST' in the Special Requirements column require step therapy before coverage of the listed product will be available. | |
| Document basis: 'if a step therapy is commonly required, it will generally be noted next to the medication with an "ST" under the Special Requirements column.' Examples in the list include antidepressant/antipsychotic entries where 'ST' is shown (e.g., levomilnacipran therapy pack = ST; aripiprazole entries list ST). |
Quantity Limits by Product (examples)
Site-of-Care and Specialty Pharmacy Notes
Verify site‑of‑care billing for provider‑administered drugs
Drugs administered by a health care professional (e.g., in hospital outpatient or clinic) may be covered under the medical benefit rather than the pharmacy benefit; verify site‑of‑care billing before submitting claims.
- Provider‑administered drugs may need to be billed to medical benefit (hospital outpatient) instead of pharmacy.
- Confirm benefit channel and billing prior to administration.
Palforzia handled via specialty program (SP)
Palforzia product levels are designated with Requirements/Limits = SP; providers must route dispensing via the specialty program and follow specialty handling processes.
- Palforzia Initial Dose and Level entries list Requirements/Limits = SP.
- Specialty program handling applies; follow specialty pharmacy procedures for dispensing.
Use specialty pharmacy for SP‑flagged agents
Many specialty/oncology oral agents are designated 'SP' indicating specialty pharmacy handling; providers must use specialty pharmacy channels for SP‑flagged drugs.
- Examples include multiple oncology agents with SP and PA flags.
- SP designation implies specialty channel dispensing and associated PA processes.
Dispense SP‑designated drugs through specialty channels
Drugs marked 'SP' must be dispensed via specialty pharmacy channels per the formulary; ensure prescriptions for SP products are routed to the specialty pharmacy.
- SP designation appears on many high‑cost and specialty products (e.g., OMNITROPE, TRIKAFTA).
- Coordinate with the specialty pharmacy for enrollment and dispensing.
Follow specialty pharmacy management for SP products
Specialty products flagged SP are managed under specialty pharmacy channels and may have additional PA and QL requirements; providers must follow specialty program processes.
- Biologics and CF therapies with SP require specialty management and PA.
- Confirm specialty pharmacy routing and PA requirements before prescribing.
Coordinate PA and specialty dispensing for SP‑flagged injectables/pens
SP‑marked drugs (including certain injectables and pens) are managed under specialty pharmacy channels and may require specialty handling and prior authorization.
- Certain auto‑injectors and pens (e.g., REPATHA pens, ZYMFENTRA auto‑injectors) are SP‑flagged.
- Coordinate PA and specialty pharmacy dispensing to secure coverage.
Definitions and Flag Key
Background and Context
Specialty drugs are used to treat complex chronic conditions and may be self‑administered or administered by a clinician. Provider‑administered specialty products given in a clinic or hospital may be covered under the medical benefit rather than the pharmacy benefit — check the plan’s site‑of‑care rules. The formulary classifies specialty agents by Drug Tier and often applies utilization controls such as PA, QL, or SP (specialty pharmacy handling) to manage access and ensure appropriate use.
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