Jubbonti (denosumab-bbdz) — HCPCS Q5136

Sandoz Inc. · 60 mg/mL single-dose prefilled syringe · subcutaneous injection · FDA-interchangeable biosimilar to Prolia

Jubbonti (denosumab-bbdz) is billed under HCPCS Q5136 at 1 unit = 1 mg, the same unit basis as reference Prolia — a 60 mg dose is 60 units. Q4 2026 ASP+6% is $26.991/1 mg unit, about 9.6% below Prolia's $29.856 in the same quarter. Jubbonti was the first denosumab biosimilar FDA-licensed as interchangeable with Prolia (March 5, 2024), and its 120 mg Xgeva-line twin, Wyost, bills the same code. Admin is a single subcutaneous injection, 96372 — not an infusion code. Nine of 27 commercial payer policies in our corpus name Jubbonti itself preferred or step-first; with Centene and Regence, which list only Wyost, Q5136 sits on 11 preferred lists, more than any other denosumab code. For the full 60 mg/120 mg product family and payer-by-payer comparison, see the denosumab biosimilars hub.

📋 Medicare coverage for denosumab — covered ICD-10 diagnoses by MAC →
CMS HCPCS:Q5136 verified Sep 2026
ASP (Q4 2026):$26.991/1 mg · live-bound to CMS file
FDA label:BLA761362, interchangeable Mar 2024
NDC:FDA NDC Directory listing 61314-240-63
Page reviewed:
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Jubbonti and Wyost share one code. Q5136 covers both the 60 mg osteoporosis product (Jubbonti) and the 120 mg oncology product (Wyost) — the billed units, not the HCPCS code, are what tell a payer which one was administered. See Jubbonti vs. Wyost.

Instant Answer — the 5 things you need to bill Jubbonti

HCPCS
Q5136
1 unit = 1 mg
Standard dose
60 units
60 mg · 1 syringe
Modifier
JZ (usual)
JW rare · TB for 340B
Admin CPT
96372
SC injection — not an infusion code
Medicare ASP+6%
$26.991
per 1 mg unit, Q4 2026 · $1,619.46/60 mg dose
HCPCS descriptor
Q5136 — "Inj. denosumab-bbdz, 1 mg" (CMS Q4 2026 ASP file); CMS Article A52399 assigns it to Jubbonti or Wyost 1 mg / unit
Biosimilar status
FDA-licensed biosimilar AND interchangeable with Prolia, both March 5, 2024. Jubbonti/Wyost held the 12-month first-interchangeable exclusivity, which ran out on October 29, 2025. BLA761362, Sandoz Inc.
Indications
Postmenopausal osteoporosis · male osteoporosis · glucocorticoid-induced osteoporosis · bone loss on aromatase-inhibitor or androgen-deprivation therapy — identical to Prolia's label. See Prolia's ICD-10 table for the full indication-to-diagnosis map.
NDC (FDA NDC Directory)
61314-240-63 (1 mL single-dose prefilled syringe) — Sandoz Inc.
Vial / syringe
60 mg/mL, single-dose prefilled syringe — matches the fixed 60 mg dose exactly, so there is normally nothing to waste
Route & administration
Subcutaneous injection (upper arm, upper thigh, or abdomen) — bills 96372 alone, no second admin code
Benefit channel
Medical (provider buy-and-bill), billed under Q5136 on the CMS-1500
Boxed warning
Same as reference Prolia: severe hypocalcemia in advanced kidney disease (eGFR under 30). See Prolia's full warnings and pre-treatment workup.
See the full payment breakdown for your patient’s dose — pre-loaded with Q5136.

The units above are the same for every patient. What this patient owes depends on their plan, deductible and any assistance they qualify for — that takes about 30 seconds to work out.

See what this patient owes →
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Admin is a single SC injection — 96372, NOT an infusion code. Jubbonti is a subcutaneous product, unlike most drugs in this reference library. Do not default to 96365/96366 or 96413/96415 out of habit from infused biologics. See administration codes.
Phase 1 Identify what you're billing Confirm interchangeable status, distinguish Jubbonti from its Wyost twin, and set the unit count for the fixed 60 mg dose.

Jubbonti is FDA-interchangeable with Prolia FDA Purple Book verified Sep 2026

Jubbonti cleared the FDA's higher interchangeable bar on the same day it was licensed as biosimilar — the first denosumab biosimilar to do so.

The FDA Purple Book gives Jubbonti one date for both approval and interchangeability: March 5, 2024. No other denosumab biosimilar was designated interchangeable before it. Being first came with a 12-month first-interchangeable exclusivity for Jubbonti and Wyost, which kept other denosumab biosimilars from launching as interchangeable. When it expired on October 29, 2025, most later products picked up that date in the Purple Book's interchangeable column. It marks the end of Jubbonti's exclusivity, not a day on which the FDA ruled on each of them. See the hub page for the full timeline across all nine pairs.

The designation does not decide payment. Whether a plan pays for Jubbonti, Prolia or another denosumab product is set by that plan's preferred-product and step rules. See payer policies.

Jubbonti vs. Wyost — one code, two doses CMS HCPCS + FDA verified Sep 2026

Sandoz markets denosumab-bbdz under two brand names for two dosing lines, and both bill the same HCPCS code, Q5136.

Jubbonti and Wyost: brand, dose line, presentation, and dosing, both under HCPCS Q5136.
BrandDose linePresentationRegimen
Jubbonti (this page) Prolia-equivalent, 60 mg 60 mg/mL single-dose prefilled syringe 60 mg subcutaneously every 6 months (osteoporosis)
Wyost Xgeva-equivalent, 120 mg 120 mg/1.7 mL (70 mg/mL) single-dose vial 120 mg subcutaneously every 4 weeks (oncology; plus Day 8 and 15 doses in month 1 for giant cell tumor of bone)

Both are denosumab-bbdz, both are Sandoz products, and both bill Q5136. Because the code does not distinguish them, the billed unit count is what separates a Jubbonti claim from a Wyost claim on the claim form: 60 units for Jubbonti, 120 for Wyost. Confirm which product was actually administered against the NDC drawn before submitting the claim — billing 60 units when the patient received Wyost, or 120 when they received Jubbonti, is the same class of error that occurs between reference Prolia and Xgeva on their shared code, J0897.

Full biosimilar family comparison. For all nine Prolia/Xgeva-line biosimilar pairs side by side — HCPCS, Medicare pricing, payer preference, and assistance status — see the denosumab biosimilars hub. This page is the Jubbonti-specific, 60 mg billing reference.

Dosing FDA label verified Sep 2026

One fixed dose, one fixed schedule — identical to reference Prolia. No induction phase and no weight-based adjustment.

Jubbonti dosing: the single fixed regimen used for every labeled indication.
IndicationRegimenNotes
All labeled indications 60 mg subcutaneously once every 6 months Postmenopausal, male, and glucocorticoid-induced osteoporosis, plus bone loss on aromatase-inhibitor or androgen-deprivation therapy.
Unit conversion: 1 unit = 1 mg, so the dose and the unit count are the same number. 60 mg = 60 units, in one syringe, every time — there is no weight-based math the way there is for an infused biologic.

Because the 60 mg fixed dose exactly matches the 60 mg fixed syringe fill, there is normally nothing left over to waste on a Jubbonti claim — see modifiers for the JZ/JW consequence of that.

NDC reference FDA NDC Directory, Sep 2026

For CMS-1500 Box 24A, pad the product segment to four digits: 61314-240-63 becomes 61314-0240-63. Check the syringe before billing.

NDC (10-digit)NDC (11-digit, claim form)Package
61314-240-6361314-0240-631 mL single-dose prefilled syringe, 60 mg/mL (Sandoz Inc.)
NDC taken from the FDA NDC Directory — not checked against drug packaging by this team. Always confirm the exact NDC printed on the syringe actually administered before submitting a claim.
Phase 2 Code the claim One subcutaneous admin code, JZ on nearly every claim, TB for 340B acquisition.

Administration codes CPT verified Sep 2026

Jubbonti is a subcutaneous injection, not an infusion. Administration bills 96372 alone.

Jubbonti is NOT infused — do not bill 96365/96366 or 96413/96415. Those codes belong to IV-infused biologics elsewhere in this reference library. Jubbonti's entire administration is one subcutaneous injection.
CPTDescriptionUse for
96372 Therapeutic, prophylactic, or diagnostic injection; subcutaneous or intramuscular The only administration code Jubbonti uses. $15.36, Medicare PFS national non-facility rate, 2026.
96365 / 96366 Therapeutic IV infusion, initial hour / each additional hour Not appropriate — Jubbonti is not infused.
96401 Chemotherapy administration, SC/IM; non-hormonal anti-neoplastic Not appropriate — denosumab-bbdz is not a chemotherapeutic agent.

Modifiers — JZ, JW, and TB (340B) CMS verified Sep 2026

JZ is the norm on essentially every Jubbonti claim because the fixed 60 mg dose exactly matches the fixed syringe size. JW is rare. TB is the sole 340B modifier.

JZ — required when no drug is discarded

Effective July 1, 2023, CMS requires the JZ modifier on all single-dose container claims when no drug is discarded. Because Jubbonti's one fixed dose (60 mg) exactly matches its one fixed syringe size (60 mg), there is normally nothing left over to waste — append JZ to the Q5136 line on essentially every claim.

JW — required for documented waste

JW applies only on the rare occasion a syringe is opened and the full 60 mg dose is not administered. Document the discarded amount in the chart and bill it on a separate line, same date of service, same HCPCS code.

TB — the only current 340B modifier

A hospital that bought Jubbonti through 340B and bills Medicare reports TB on the Q5136 line. JG has not been used since CMS discontinued it on January 1, 2025.

Modifier 25 — same-day E/M

Append modifier 25 to the same-day E/M code only if a significant, separately identifiable evaluation occurred beyond the routine pre-injection check-in, which is bundled into the administration code.

ICD-10-CM codes for Jubbonti and Wyost claims Codes as on our Prolia and Xgeva pages

The diagnosis in Box 21 should match the product drawn: a bone-loss code for a 60-unit Jubbonti line, a cancer code for a 120-unit Wyost line.

Jubbonti, 60 mg (osteoporosis and treatment-related bone loss)

IndicationICD-10Add or note
Postmenopausal osteoporosisM81.0No current pathological fracture
Male osteoporosisM81.8Other osteoporosis
Glucocorticoid-induced osteoporosisM81.8Add Z79.52 (long-term systemic steroids)
Bone loss on aromatase-inhibitor therapyZ85.3Add Z79.811; add M81.0 if osteoporosis is confirmed
Bone loss on androgen-deprivation therapyZ85.46Add Z79.899; add M81.8 if osteoporosis is confirmed
Osteoporosis with current pathological fractureM80.0xx- / M80.4xx- / M80.8xx-Seventh character for initial vs. subsequent encounter
Localized osteoporosis (Lequesne)M81.6Uncommon

Wyost, 120 mg (oncology)

IndicationICD-10Add or note
Bone metastases from a solid tumorC79.51Add the primary cancer code, or a Z85.x history code
Secondary involvement of bone marrowC79.52Add the primary cancer code
Multiple myelomaC90.00C90.01 in remission, C90.02 in relapse
Giant cell tumor of boneD48.0
Hypercalcemia of malignancyE83.52Add the primary cancer code

Hypocalcemia, E83.51, is a reason to hold a dose, not a reason to give one, so never put it on a Q5136 line as the diagnosis. Jubbonti's full indication notes live on the Prolia page, and Wyost's on the Xgeva page.

Claim form field mapping CMS-1500 field reference

CMS-1500 / 837P (physician office; POS 11) example for a standard 60 mg Jubbonti dose.

InformationCMS-1500 boxNotes
NDC qualifier + 11-digit NDC + UoM + qty24A shaded areaFormat: N4 qualifier + 11-digit NDC + UN + quantity drawn (1 syringe)
HCPCS Q5136 + JZ (JW only if waste)24D (drug line)60 units for Jubbonti, 120 for Wyost
CPT 9637224D (admin line)One line — no second admin code
ICD-1021Osteoporosis / bone-loss indication — see ICD-10 codes
PA number (when required)23Required by many payers — see payer policies
TB modifier (340B sites only)24DHospital 340B claims to Medicare
Phase 3 Get paid Nine payers in our corpus prefer Jubbonti. Anthem, Excellus and UnitedHealthcare list it as non-preferred.

Payer policy snapshot — who prefers Jubbonti Reviewed Sep 2026, 27-payer corpus

Jubbonti itself is preferred or step-first in 9 of the 27 commercial payer policies surveyed. Two more prefer only its 120 mg twin, Wyost.

Preferred for Jubbonti (60 mg line): BCBS Louisiana, BCBS Massachusetts, BCBS Minnesota, BCBS Nebraska, BCBS South Carolina, Blue Shield of California, Florida Blue, Independence Blue Cross, and Wellmark BCBS. Preferred for Wyost only (120 mg line): Centene/Ambetter and Regence BCBS. Their preferred lists name Wyost and do not name Jubbonti.

Several of the nine make other products wait behind Jubbonti. BCBS Louisiana, for example, approves Prolia, Stoboclo or Conexxence only after the patient has tried and failed Jubbonti, Bildyos and Enoby. Going the other way, Jubbonti is non-preferred at Anthem (which prefers Prolia), Excellus (which prefers Bildyos and Enoby) and UnitedHealthcare.

UnitedHealthcare is the exception. UHC's preferred denosumab products are Prolia and Stoboclo (Q5157), not Jubbonti. To approve Jubbonti, UHC's criteria call for either an adequate trial of both Prolia and Stoboclo with minimal clinical response (plus physician attestation of an expected superior response to Jubbonti), or a history of intolerance, contraindication or adverse event with both.

Jubbonti is not on BCBS Mississippi's covered list. Per the payer's policy, the covered denosumab products are Stoboclo/Osenvelt, Bildyos/Bilprevda and Enoby/Xtrenbo, and biosimilars it does not name are non-formulary. Our copy of that policy is filed under a web address for a different policy, so call BCBS Mississippi before scheduling a Jubbonti patient there.

See the full payer-by-payer comparison across all nine biosimilar pairs on the denosumab biosimilars hub.

Medicare reimbursement CMS Q4 2026 (live)

Quarterly ASP from the CMS Part B Drug Pricing File.

Q4 2026 payment snapshot — Q5136 Jubbonti

Effective October 1 – December 31, 2026

ASP + 6%
$26.991
per 1 mg unit
60 mg dose
$1,619.46
60 units × ASP+6%
vs. reference Prolia
~9.6% lower
$29.856 J0897 · same quarter

With the 96372 administration allowance ($15.36, 2026 Medicare PFS national non-facility rate) added, a 60 mg Jubbonti claim totals $1,634.82 before sequestration, against $1,806.72 for the equivalent Prolia claim.

Coverage

CMS MCD Article A52399 ("Billing and Coding: Denosumab and biosimilars") lists Q5136 for Jubbonti or Wyost. For the MAC-level ICD-10 ranges, see Medicare covered diagnoses for denosumab.

Canonical code source: CMS HCPCS quarterly update file.

Patient assistance — Sandoz programs Status checked Sep 12, 2026

Sandoz One Source Co-Pay Program is open: eligible commercially insured patients may pay as little as $0 for Jubbonti. Medicare, Medicaid and other government coverage are excluded, and it covers the drug only, not the administration. Verify current terms at sandoz-onesource.com/jubbonti before quoting a figure to a patient.

Sandoz Patient Assistance Program: closed for Jubbonti, and not fully settled. Our record lists it as closed. Sandoz's patient-services page gives application instructions only for Zarxio and Tyruko, and jubbonti.com documents only the co-pay program. The record's "free drug" wording describes what the program would give if Jubbonti qualified, not a benefit you can get today. The Sandoz record for Wyost is flagged unsettled until someone confirms it by phone, so call Sandoz before sending a patient to it.
Need to model what a specific patient will actually pay after copay assistance, deductible, coinsurance, and OOP max? Run a CareCost Estimate — Q5136 pre-loaded.
Phase 4 Fix problems Top three: wrong admin code, wrong unit count between Jubbonti and Wyost, wrong HCPCS billed against the NDC drawn.

Common denials & how to fix them

Denial reasonCommon causeFix
Wrong admin code (infusion code used) Biller defaulted to 96365/96366 or 96413/96415 out of habit from infused biologics Resubmit with 96372 — the only administration code Jubbonti bills.
Wrong unit count (60 vs. 120) Wyost's 120 mg dose billed under a Jubbonti claim, or vice versa — both share Q5136 Confirm which product was actually administered against the NDC drawn and bill the matching unit count.
Wrong HCPCS (J0897 or another biosimilar code billed) Reference Prolia or a different biosimilar billed when the patient received Jubbonti Match the HCPCS to the NDC actually drawn: 61314-240 series = Jubbonti.
JZ missing Single-dose-syringe claim without JZ when no drug was discarded Resubmit with JZ on the Q5136 line — the norm on nearly every Jubbonti claim.
Step-therapy documentation missing (UHC) Jubbonti billed at UnitedHealthcare without a documented trial of Prolia and Stoboclo Submit trial-and-failure or intolerance documentation for both Prolia and Stoboclo per UHC's policy, or confirm PA before scheduling.
Assumed interchangeable substitution occurred at the pharmacy Claim or record implies a retail-style automatic swap between Jubbonti and Prolia For a medical-benefit, buy-and-bill drug, confirm which product the prescriber specifically ordered and which product payer policy actually approved — the interchangeable designation does not bypass payer preference.

Frequently asked questions

What is the HCPCS code for Jubbonti?

Jubbonti (denosumab-bbdz) is billed under HCPCS Q5136, billed 1 unit = 1 mg, the same unit basis as reference Prolia (J0897). The standard 60 mg osteoporosis dose is 60 units.

Is Jubbonti interchangeable with Prolia?

Yes. The FDA Purple Book lists Jubbonti as interchangeable with Prolia from March 5, 2024, the day it was approved, which made it the first interchangeable denosumab biosimilar. Each plan's preferred-product rules still decide which denosumab product gets paid.

What is Wyost, and does it bill the same code as Jubbonti?

Wyost is the 120 mg Xgeva-line twin of Jubbonti — same manufacturer (Sandoz), same active ingredient (denosumab-bbdz), same HCPCS code, Q5136. Jubbonti is dosed 60 mg subcutaneously every 6 months for osteoporosis; Wyost is dosed 120 mg every 4 weeks for oncology indications. The units on the claim, 60 versus 120, are what separate them, since both bill Q5136.

Which payers prefer Jubbonti (Q5136)?

Nine of the 27 commercial payer policies in our corpus prefer Jubbonti: BCBS Louisiana, BCBS Massachusetts, BCBS Minnesota, BCBS Nebraska, BCBS South Carolina, Blue Shield of California, Florida Blue, Independence Blue Cross and Wellmark BCBS. Centene/Ambetter and Regence BCBS prefer only Wyost, the 120 mg product on the same code. UnitedHealthcare prefers Prolia and Stoboclo and wants a trial of both before approving Jubbonti.

What is the Q4 2026 Medicare reimbursement for Q5136?

Q4 2026 ASP+6% for Q5136 Jubbonti is $26.991 per 1 mg unit — about 9.6% below reference Prolia's $29.856 in the same quarter. A 60 mg dose is 60 units, pricing to $1,619.46 before the administration allowance and sequestration.

Is manufacturer assistance available for Jubbonti?

For commercially insured patients, yes: the Sandoz One Source Co-Pay Program is open, with costs as low as $0 (Medicare, Medicaid and other government plans excluded). The Sandoz Patient Assistance Program, the free-drug route, is closed for Jubbonti in our record, because its application instructions name only Zarxio and Tyruko. Confirm with Sandoz before referring a patient.

Reference Sources & methodology Every claim on this page is sourced. Methodology and review history below.

Source documents

  1. FDA Purple Book Database — full monthly data file, August 2026 release
    BLA761362; approval and interchangeable-designation date; reference product
  2. DailyMed — JUBBONTI (denosumab-bbdz) prescribing information
    Presentation; labeled dose and interval
  3. openFDA NDC Directory — denosumab listings
    NDC 61314-240-63 and its marketing start date
  4. CMS MCD Article A52399 — Billing and Coding: Denosumab and biosimilars
    HCPCS Q5136 descriptor and code verification
  5. CMS — Medicare Part B Drug ASP Pricing File
    Q4 2026 quarterly file (Q5136, J0897)
  6. CMS — Medicare Part B inflation rebate guidance: use of the 340B modifier
    JG modifier discontinued for all 340B-covered entities effective January 1, 2025; TB is the sole 340B modifier
  7. Sandoz One Source — Jubbonti co-pay program
    Co-pay assistance program terms and enrollment
  8. CareCost Estimate — Prolia reference (J0897 and the full denosumab biosimilar family)
    ICD-10 by indication, boxed warnings, pre-treatment workup, MUE
  9. CareCost Estimate — Denosumab biosimilars hub
    Full nine-pair comparison, payer-by-payer preference split, price spread

About this page

Medicare ASP pricing for Q5136 is bound to our underlying CareCost data layer and refreshes automatically when CMS publishes new quarterly files. Coding, payer-policy, and assistance-program content is reviewed at least quarterly and updated whenever the manufacturer program, FDA label, or a major payer policy changes.

Found an error? Email hello@carecostestimate.com.

Refresh cadence

ElementCadenceHow it's refreshed
Medicare ASP pricingQuarterlyAuto-bound to CareCost ASP layer; updates on CMS file release.
Payer policiesSemi-annualManual review against published payer policy documents.
Assistance program statusAnnual, or on manufacturer changeReviewed against the manufacturer's own program pages.
HCPCS / CPT / NCCI rulesAnnualReviewed against CMS HCPCS quarterly files and AMA CPT releases.
NDC, dosing, FDA labelEvent-drivenTied to the DailyMed structured product listing and FDA label revision date.

Reviewer

Reviewed by Erin Rose, CareCost Estimate founder. Figures come from the FDA Purple Book, DailyMed, CMS quarterly ASP files, and payer policy documents, cited inline. See our methodology and editorial policy. Found an error? Report it.

Change log

  • — Initial publication. Jubbonti-specific (Q5136) billing reference: interchangeable-status framing, NDC 61314-240-63 from the FDA NDC Directory, single subcutaneous admin code (96372), JZ/JW/TB modifier guidance, the Wyost 120 mg twin on the same code, 2026 payer preference snapshot (9 of 27 payers for Jubbonti, 2 more for Wyost only), and Sandoz One Source assistance status.

Methodology

Every claim on this page is sourced inline. The NDC comes from the FDA NDC Directory and dosing from the DailyMed label; the ASP figure is read live from the CMS Part B ASP file; payer rules are read from each plan's published medical policy; assistance-program status is read from the manufacturer's own program page. We do not paraphrase from billing-software vendor blogs, and we flag anything not yet SME-verified rather than assert it.

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