Summary & Overview
HCPCS J0517: Injection, benralizumab, 1 mg
HCPCS Level II code J0517 designates a 1 mg unit of benralizumab, a monoclonal antibody administered by injection for management of certain eosinophilic respiratory conditions. As a drug-specific HCPCS code, J0517 is used on medical claims to report the billed quantity of benralizumab supplied and is central to pharmacy-oncology and specialty drug reimbursement workflows nationwide. The code matters nationally because biologic therapies represent high-cost, high-impact services with complex coverage and utilization controls across payers.
Key payers covered in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of clinical context for benralizumab use, the service setting and billing implications for injectable biologics, and what to expect in payer coverage policies and billing practice. The publication summarizes common billing considerations, typical sites of service and service line implications, and provides benchmarks and policy-relevant issues where available. Data not available in the input will be noted explicitly where necessary.
Billing Code Overview
HCPCS Level II code J0517 represents an injection of benralizumab, 1 mg. The service type is therapeutic monoclonal antibody administration used for subcutaneous or injectable biologic therapy. The typical site of service is outpatient infusion/clinic or physician office settings where biologic injections are administered.
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Clinical & Coding Specifications
Clinical Context
A typical patient is an adult with severe eosinophilic asthma or eosinophilic chronic rhinosinusitis refractory to standard inhaled corticosteroids and bronchodilators who is scheduled to receive subcutaneous benralizumab therapy. The patient presents to an outpatient infusion or injection clinic, allergy/immunology office, or pulmonology clinic for administration of J0517 (benralizumab, 1 mg). The clinical workflow includes verification of patient identity and insurance, review of indications and recent clinical status (exacerbation frequency, oral corticosteroid use, blood eosinophil count), documentation of any prior biologic therapy and allergic reactions, and assessment of injection site and vitals. The medication is prepared as the appropriate mg dose (per product dosing schedule), administered subcutaneously, and the patient is observed for immediate hypersensitivity or injection-site reaction per office protocol (commonly 30 minutes for first dose, shorter for maintenance doses if tolerated). Nursing documents lot number, expiration, dose administered, route (subcutaneous), site (e.g., right deltoid), and applicable modifier if required by the payer. Follow-up includes scheduling the next dose per dosing interval and documenting clinical response and any adverse events.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
JW | Drug amount discarded/not administered | Use when partial vial is discarded after administration and payor requires reporting of wasted drug. |