Summary & Overview
HCPCS J2351: Ocrelizumab with Hyaluronidase Injection, 1 mg
HCPCS Level II code J2351 denotes the injection of ocrelizumab, 1 mg, combined with hyaluronidase-ocsq. The code identifies a therapeutic biologic administration relevant to neurology and infusion therapy practices and is used in billing for outpatient infusion or clinic-based injectable services. Nationally, accurate coding for high-cost biologics such as ocrelizumab affects payer reimbursement, care coordination, and drug utilization tracking.
Key payers covered include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find benchmarks and clarity on clinical context for use of this HCPCS Level II code, common billing considerations, and the typical sites where the service is provided. The publication outlines how J2351 is applied in billing lines, highlights common modifiers and payer reporting conventions (where available), and summarizes implications for billing workflows and claims processing. Data not available in the input is noted where relevant.
Billing Code Overview
HCPCS Level II code J2351 represents an injection of ocrelizumab, 1 mg, combined with hyaluronidase-ocsq. This code is used to report administration of the specified biologic agent preparation for infusion or injection therapy.
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Service type: Therapeutic biologic injection
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Typical site of service: Infusion center or outpatient clinic setting where injectable biologic therapies are administered
Clinical & Coding Specifications
Clinical Context
A patient with relapsing-remitting multiple sclerosis or primary progressive multiple sclerosis presents to an infusion center for administration of J2351 (injection, ocrelizumab, 1 mg and hyaluronidase-ocsq). The typical patient is an adult who has been evaluated by a neurologist and whose treatment plan specifies subcutaneous ocrelizumab combined with hyaluronidase to facilitate absorption. The clinical workflow includes pre-infusion screening (vital signs, review of prior infusion reactions, pregnancy testing where indicated, screening for active infections and hepatitis B), verification of consent and dosing, preparation of the medication by pharmacy, administration by an infusion or injection nurse, observation for infusion or injection-related reactions for the recommended post-administration period, and documentation of lot numbers, dose administered, site of injection, and any adverse reactions. Orders and documentation commonly include start/stop times, modifier reporting for billing, and coordination of future dosing intervals per the treating neurologist’s protocol.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
JW | Drug discarded/not administered to any patient | Use when a portion of the single-use vial is discarded and must be reported for tracking of wasted drug cost. |