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HCPCS Code

HCPCS code J3262 – Tocilizumab injection


Code Definition

J3262 is the HCPCS Level II code for injection, tocilizumab, 1 mg. It bills intravenous Actemra for rheumatoid arthritis, giant cell arteritis, two forms of juvenile idiopathic arthritis, cytokine release syndrome and hospitalized COVID-19.

Units follow the milligrams infused, so a 280 mg dose bills 280 units. Subcutaneous Actemra is mostly self-injected and covered under Part D instead. Each biosimilar has its own code: Q5133 for Tofidence, Q5135 for Tyenne and Q5156 for Avtozma.

Level
Level II
Category
J – Drugs administered other than oral method
Status
Active
Billable
No
Code also known as
Actemra infusion, tocilizumab IV, IL-6 receptor antagonist injection
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Key takeaways

Key takeaways

J3262 bills intravenous tocilizumab (Actemra) per 1 mg, so units equal the milligrams infused, not the vials opened.

RA starts at 4 mg/kg every 4 weeks, so a 70 kg patient’s 280 mg dose bills 280 units.

Medicare Part B pays J3262 at ASP plus 6%, and every single-dose vial line needs the JZ or JW modifier.

Biosimilars bill under their own Q-codes: Q5133 for Tofidence, Q5135 for Tyenne and Q5156 for Avtozma.

Claims software such as Pabau pre-fills the claim form from the patient record and checks required fields before submission.

HCPCS code J3262 bills IV tocilizumab per milligram

HCPCS code J3262 is the Level II drug code for injection, tocilizumab, 1 mg. Practices use it to bill intravenous Actemra, the IL-6 receptor antagonist from Genentech, a member of the Roche Group. One unit equals one milligram administered, for Medicare, Medicaid and most commercial plans.

Actemra won FDA approval in January 2010. J3262 took effect on January 1, 2011, replacing C9264, the temporary code used during 2010.

FieldValue
HCPCS codeJ3262
Official descriptorInjection, tocilizumab, 1 mg
Brand nameActemra (Genentech)
Drug classIL-6 receptor antagonist (monoclonal antibody)
Administration routeIntravenous infusion; subcutaneous doses are mostly self-injected under Part D
Billing unitPer 1 mg administered
In use sinceJanuary 1, 2011 (replaced C9264)
Biosimilar codesQ5133 (Tofidence), Q5135 (Tyenne), Q5156 (Avtozma)
Code setHCPCS Level II (maintained by CMS)

J3262 sits in the HCPCS Level II J series, which covers drugs administered other than by mouth. CMS maintains the HCPCS Level II code set and publishes updates every quarter.

Six FDA-approved uses set the ICD-10 code

Payers match the diagnosis on a J3262 claim against the FDA label and their own clinical policy. IV tocilizumab has six approved indication groups, and each one maps to its own ICD-10 codes.

IndicationKey ICD-10 codesPA commonly required?
Rheumatoid arthritis (RA)M05.79, M05.9, M06.00, M06.9Yes, by most commercial payers
Polyarticular juvenile idiopathic arthritis (PJIA)M08.3; M08.0- (unspecified juvenile rheumatoid arthritis)Yes
Systemic juvenile idiopathic arthritis (SJIA)M08.20, M08.29Yes
Giant cell arteritis (GCA)M31.5, M31.6Yes, and step therapy may apply
Cytokine release syndrome (CRS)D89.831, D89.832, D89.839Typically not (urgent inpatient setting)
COVID-19 in hospitalized adultsU07.1Rarely (inpatient use)

Seronegative polyarticular disease codes to M08.3. The M08.4- codes describe pauciarticular disease, so they do not support a PJIA claim.

Off-label use is not covered by every commercial payer. Coverage varies by plan and policy year, so confirm the payer’s criteria before you infuse for an unlisted indication.

J3262 units equal the milligrams you infuse

J3262 is billed per 1 mg, so the unit count equals the total milligrams administered. The dose comes from the patient’s weight and the indication’s schedule on the FDA label:

  • RA: 4 mg/kg every 4 weeks, which may increase to 8 mg/kg. No more than 800 mg per infusion.
  • GCA: 6 mg/kg every 4 weeks with tapering glucocorticoids. No more than 600 mg per infusion.
  • PJIA: 10 mg/kg under 30 kg, or 8 mg/kg at 30 kg and above, every 4 weeks.
  • SJIA: 12 mg/kg under 30 kg, or 8 mg/kg at 30 kg and above, every 2 weeks.
  • CRS: 12 mg/kg under 30 kg, or 8 mg/kg at 30 kg and above. No more than 800 mg per infusion.
  • COVID-19: a single 8 mg/kg infusion, up to 800 mg. One more dose may follow at least 8 hours later.

The calculation itself takes three steps:

  • Step 1: Confirm the patient’s weight in kilograms from the clinical record.
  • Step 2: Multiply weight by the prescribed mg/kg dose, then apply the label’s per-infusion cap.
  • Step 3: Bill that total as the number of J3262 units, without rounding up to the next vial.

Worked examples for a 70 kg patient

Dose levelCalculationJ3262 units to bill
4 mg/kg (RA start)70 kg x 4 mg/kg = 280 mg280 units
6 mg/kg (GCA)70 kg x 6 mg/kg = 420 mg420 units
8 mg/kg (RA after increase)70 kg x 8 mg/kg = 560 mg560 units

The cap matters for heavier patients. A 110 kg RA patient at 8 mg/kg calculates to 880 mg, but the label limits the infusion to 800 mg. That claim carries 800 units.

Vials, waste and the JW or JZ modifier

Actemra IV comes in 80 mg, 200 mg and 400 mg single-dose vials. Medicare Part B wants a waste modifier on every single-dose vial drug line. Use JZ when no drug was discarded.

When some drug is discarded, bill the administered milligrams on one line. Then bill the discarded milligrams on a second J3262 line with JW, and record the discarded amount in the note. The vial mix decides which case applies, as these two infusions show.

Two J3262 claim examples for a 70 kg patient
At 8 mg/kg the vials empty exactly, so one JZ line covers the dose. At 6 mg/kg, 20 mg is left over and needs its own JW line. Doses follow the Actemra label and modifiers follow CMS JW and JZ policy.

Pro Tip

Document the patient’s weight, the prescribed dose in mg/kg, and the calculated total mg in the infusion note on every encounter. If the clinical record and the billed unit count cannot be reconciled in 30 seconds during an audit, expect a recoupment demand.

The infusion itself bills under separate CPT codes

J3262 covers the drug only, so the infusion service goes on its own line with a CPT administration code. CPT guidelines let the chemotherapy administration codes report monoclonal antibody infusions. That is why tocilizumab infusions are often billed with 96413, timed against the start and stop times in the note.

CPT codeDescriptionWhen to use
96413Chemotherapy administration, IV infusion, initial up to 1 hourFirst hour of the tocilizumab infusion, since CPT treats monoclonal antibodies as complex drugs for these codes
96415Chemotherapy administration, IV infusion, each additional hourOne unit per additional hour of infusion time beyond the first
96365IV infusion, therapeutic/prophylactic, initial up to 1 hourSome payers prefer this code over 96413 for non-cancer biologics, so check payer policy
96366IV infusion, each additional hourAdditional hours when 96365 is the initial code

Do not bill IV hydration (96360/96361) on the same date unless it is a clinically distinct service with its own documented reason. Bundling edits reject a standalone hydration line attached to a tocilizumab infusion claim.

Medicare pays J3262 at ASP plus 6%

Medicare Part B pays J3262 at the average sales price (ASP) plus 6%. That holds in the physician office and in the hospital outpatient department, where tocilizumab is separately payable under OPPS. CMS updates ASP payment limits every quarter, so the rate changes four times a year.

Tocilizumab is a high-cost biologic, so a small ASP change still moves revenue. Pull the current limit from the CMS ASP pricing files at the start of each quarter. Part B drug payment comes from that file, not from the Physician Fee Schedule.

Office and hospital claims follow different rules

FactorPhysician office / infusion suiteHospital outpatient department
Payment methodASP + 6% per unitASP + 6% per unit, separately payable under OPPS
Claim formCMS-1500UB-04
Place of service code11 (office)19 (off-campus) or 22 (on-campus) on the professional claim
NDC reportingMedicaid and many commercial payers; Medicare for dual-eligible patientsPer payer; required by Medicaid
340B modifierTB on 340B-acquired drug lines, for covered entities onlyTB on 340B-acquired drug lines (JG retired after December 31, 2024)

Medicare does not require the NDC on most Part B claims, except for patients who are dually eligible for Medicaid. Medicaid and many commercial payers do require it.

They expect the N4 qualifier, the 11-digit NDC, a unit qualifier such as UN and the quantity. A missing or malformed NDC is one of the most common reasons these claims bounce.

Buy-and-bill decides whether you bill the drug at all

Most infusion practices buy tocilizumab and bill it themselves. Under buy-and-bill, the practice purchases the drug, administers it and bills the payer for both the drug and the infusion.

  • Buy-and-bill: The practice buys from a specialty distributor and bills J3262 plus the administration codes on a CMS-1500. This model needs NDC tracking and drug cost reconciliation.
  • Specialty pharmacy (white bagging): The payer has a specialty pharmacy ship the drug to the practice for one patient. The practice never owns the drug, so it bills the administration codes only, not J3262. Check payer contracts before you accept a white-bagging policy, because the revenue impact is large.
  • Brown bagging: The patient brings the drug from a pharmacy to the infusion site. The practice bills administration only, and many practices decline this model over safety and liability concerns.

340B covered entities buy tocilizumab at the 340B ceiling price, well below ASP. After the Supreme Court ruled in AHA v. Becerra in 2022, CMS restored payment for 340B-acquired drugs to ASP plus 6% from 2023.

Since January 1, 2025, every 340B covered entity reports modifier TB on 340B-acquired drug lines, and JG is retired. CMS uses the modifier to keep 340B units out of Part B inflation rebates.

Prior authorization comes before the first infusion

Most commercial payers and many Medicare Advantage plans require prior authorization (PA) before the first J3262 infusion.

Traditional Medicare does not require PA for office-administered drugs, but Medicare Advantage plans set their own rules. Completing insurance eligibility verification before scheduling shows which plan type applies and whether PA is needed.

Published payer policies for RA and GCA commonly ask for the following:

  • A confirmed diagnosis with the supporting ICD-10 code documented
  • Step therapy, usually a trial of at least one conventional DMARD such as methotrexate
  • A rheumatologist or other appropriate specialist as the prescriber
  • Baseline labs (CBC, liver function tests, lipids) documented before treatment starts
  • For GCA, a temporal artery biopsy or vascular imaging report

PA criteria differ by payer and change with each plan year. Confirm current requirements with the payer’s PA department or provider portal before you submit.

Subcutaneous tocilizumab usually bills under Part D

J3262 claims in practice cover IV infusions. Subcutaneous Actemra comes as a 162 mg prefilled syringe and autoinjector, and patients mostly inject it at home. Medicare covers self-administered doses under Part D, so they rarely reach a medical claim.

FactorIV tocilizumabSubcutaneous tocilizumab
How the drug is billedJ3262 on the medical claimUsually dispensed by a pharmacy under Part D; check payer policy for an office-given dose
Administration CPT96413 / 96415 or 96365 / 96366 (IV infusion)96372 (SC or IM injection)
SettingInfusion suite or hospital outpatientMostly home, self-administered
Medicare coveragePart B (physician-administered drug)Typically Part D when self-administered

An SC dose billed with IV infusion codes is a route mismatch, and payers deny or return it. Payer remark codes vary, so read the ERA before you correct and resubmit.

Each tocilizumab biosimilar has its own Q-code

Three tocilizumab biosimilars are FDA-approved in the United States. Each one bills under its own HCPCS Level II code, and each is billed per 1 mg, so the unit math stays the same. The NDC on the vial tells you which code belongs on the line.

ProductManufacturerHCPCS codeFormulations
Actemra (tocilizumab)Genentech (Roche)J3262Reference product; IV and SC
Tofidence (tocilizumab-bavi)Bio-Thera Solutions; US rights held by OrganonQ5133IV
Tyenne (tocilizumab-aazg)Fresenius KabiQ5135IV and SC
Avtozma (tocilizumab-anoh)CelltrionQ5156IV and SC

Billing a biosimilar under J3262 sends the wrong product to the payer and skews ASP data. CMS adds new Q-codes through its quarterly HCPCS updates, so check the file whenever a new product reaches your shelf.

How a J3262 claim moves from chair to payment

A clean J3262 claim is built across five handoffs. Each one feeds the next, so an error early on shows up as a denial weeks later.

  1. Before the visit: Front desk staff verify coverage and confirm the PA number covers this indication and date.
  2. During the infusion: The nurse records weight, dose, vial NDCs, discarded milligrams, and start and stop times.
  3. Coding: The coder builds the J3262 line with units and JZ or JW, plus the administration code and diagnosis.
  4. Submission: The claim goes out on a CMS-1500 or UB-04, with the NDC and any TB modifier the payer needs.
  5. Follow-up: Billing staff post the ERA, compare paid units to billed units and work any denial line by line.

Why J3262 claims get denied

J3262 claims fail for a predictable set of reasons. Structured denial management that tracks remark codes by denial type shows which issue drives volume, so you can fix the cause once.

  • Missing or invalid NDC: Payers that require it expect 11 digits in 5-4-2 format with a unit qualifier. A malformed NDC usually returns a missing-information denial.
  • Missing JZ or JW: Medicare Part B lines for single-dose vials need one of the two modifiers.
  • PA not obtained or expired: The PA number is absent or wrong, or it covers a different indication than the one billed.
  • Diagnosis not covered: The ICD-10 code is not on the payer’s approved list, which is common with off-label use.
  • Incorrect unit count: Billed units do not match the documented dose, or they exceed the label cap.
  • Route mismatch: An SC dose is billed with IV infusion codes instead of 96372.
  • Wrong place of service: POS 22 or 19 appears on an office claim. Office infusion suites use POS 11.
  • 340B modifier missing: A covered entity omits TB on a 340B-acquired line, which creates audit risk more often than an upfront denial.
  • Bundling errors: IV hydration is billed on the same date without a clinically distinct reason.

The infusion note has to back every claim field

Any J3262 claim can be pulled for post-payment review, and audit-ready records cost less than rebuilding them later. Practices that build medical billing compliance habits around infusion claims tend to see fewer recoupments.

The infusion note needs each of these to support a J3262 claim:

  • The confirmed diagnosis with its ICD-10 code, documented by the treating physician
  • Drug name (generic and brand), lot number, NDC and vial strengths used
  • The prescribed mg/kg dose and the calculated total milligrams administered
  • Any discarded milligrams, which support the JW line
  • Infusion start and stop times, which support the administration units
  • The patient’s weight on or near the date of service
  • Monitoring notes, including adverse events and vital sign checks
  • Prescribing and administering provider credentials
  • The PA number and approval date where PA was required

A clean claim submission for J3262 depends on the note and the claim form agreeing field by field. A gap between the documented dose and the billed units is the most common trigger for an individual claim audit.

Pro Tip

Run a monthly reconciliation report comparing billed J3262 units against documented infusion weights and doses. A spreadsheet that cross-checks the documented dose against the claim line takes 30 minutes to build. It catches calculation errors before they become audit findings.

Before you submit a J3262 claim, check these

Run through this list on every tocilizumab claim before it leaves the practice:

  • Units equal the milligrams administered, within the label cap
  • JZ is on the drug line, or a separate JW line carries the discarded milligrams
  • The code matches the product: J3262 for Actemra, the Q-code for a biosimilar
  • The diagnosis matches an approved indication and the PA on file
  • The administration code matches the route and the documented infusion time
  • POS 11 is on an office claim, and the NDC is present where the payer requires it
  • TB is on any 340B-acquired drug line

How Pabau keeps J3262 claim data consistent

A J3262 claim usually breaks where data gets retyped. The dose comes from the infusion note, the diagnosis from the chart and the PA number from a payer portal.

Pabau, the practice platform we build, includes billing software for rheumatologists and other infusion teams. It pre-fills the claim form from the patient record, so recorded diagnoses and service codes land on the claim. Staff can search ICD-10 and CPT/HCPCS code libraries without leaving the claim screen.

Required fields, such as the member ID and authorization number, must be complete before the claim can be sent. US claims go out through Claim.MD with real-time eligibility checks, and ERA remittances post back against each claim. Your team spends its time checking units and modifiers instead of copying data between screens.

Pabau claims management screen for preparing an insurance claim
Pabau’s claims screen pre-fills the form from the patient record, so staff review J3262 units and diagnosis codes instead of retyping them.

Send cleaner J3262 claims with Pabau

Pabau pre-fills the claim form from the patient record and checks required fields before you send it. US claims go through Claim.MD with eligibility checks and ERA posting.

Pabau claims management dashboard

Conclusion

Treat every J3262 claim as a milligram calculation that has to survive an audit. The weight, the dose, the vials and the discarded amount have to agree across the note and the claim. When they do, Medicare pays at ASP plus 6% without a fight.

The biosimilar question is settled, so let the NDC on the vial pick between J3262 and the three Q-codes. The trade-off worth remembering is time. A two-minute check before submission costs far less than a recoupment months later.

Book a demo to see how Pabau turns a documented infusion into a complete J3262 claim.

Continue your research

Continue your research

Need a framework for managing denied infusion claims? Denial management in healthcare walks through the systematic approach to tracking, appealing, and preventing claim rejections.

Billing the infusion with the therapeutic codes instead? CPT code 96365 covers initial IV infusion billing, add-on hours and reimbursement.

Giving a dose by subcutaneous injection? CPT code 96372 explains injection billing, modifiers and payment.

Billing Medicare for the first time? Medicare billing for practices covers the models, claiming channels and compliance rules.

Want to understand the full revenue cycle for infusion services? What is revenue cycle management explains how every billing workflow step connects from eligibility check to final payment.

Frequently asked questions about HCPCS code J3262

Which Actemra vial sizes bill under J3262?

Actemra IV comes in 80 mg, 200 mg and 400 mg single-dose vials, each at 20 mg/mL. Pharmacy can combine vials to match any dose. The claim still carries one J3262 unit per milligram given, whatever mix of vials was opened.

How often can J3262 be billed?

That depends on the indication. RA, GCA and PJIA infusions run every 4 weeks, while SJIA runs every 2 weeks. Payers apply frequency edits, so a claim that arrives earlier than the label interval usually needs supporting documentation.

Is J3262 paid separately for an inpatient COVID-19 dose?

No. Medicare pays drugs given during a covered inpatient stay inside the hospital’s MS-DRG payment. A tocilizumab dose for a hospitalized COVID-19 patient is not paid as a separate J3262 line under Part A.

Does J3262 need a modifier?

On Medicare Part B, yes. Every single-dose vial line needs JZ when nothing was discarded, or a separate JW line for discarded milligrams. Add TB when a 340B covered entity acquired the drug through the program.

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Monika Lazarevska
Content Writer

Monika Lazarevska writes content for owners and healthcare professionals who want clear, no-fluff content that actually helps them run their practice better. With a background in storytelling and SEO, she knows how to make even the driest topics worth reading. Off the clock, you'll find her in a café somewhere in Europe, probably with a good book and an even better coffee.
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