Vyepti (eptinezumab-jjmr) — HCPCS J3032

H. Lundbeck A/S · 100 mg/mL single-dose vial · IV infusion (~30 min) · Migraine prevention in adults (episodic + chronic)

Vyepti is the only IV anti-CGRP monoclonal antibody for migraine prevention, billed under HCPCS J3032 at 1 mg per unit. Two flat-dose options: 100 mg every 3 months (100 units, recommended starting dose) or 300 mg every 3 months (300 units, for patients requiring escalation). Only 4 infusions per year — major adherence advantage over monthly SC anti-CGRPs. JZ modifier required on virtually every claim (single-dose vials, no waste). Q2 2026 Medicare reimbursement: $20.546/mg ($2,054.60 per 100 mg dose, ASP + 6%). Step therapy from oral prophylactics + at least one SC anti-CGRP is the norm on commercial PA.

ASP data:Q2 2026 (live)
Payer policies:verified May 2026
Manufacturer guide:Lundbeck 2026
FDA label:revised 2025
Page reviewed:

Instant Answer — the 5 things you need to bill J3032

HCPCS
J3032
1 mg = 1 unit
Standard dose
100 units
100 mg q3 months
Modifier
JZ
Required (single-dose vial, no waste)
Admin CPT
96365
Therapeutic IV (non-chemo, ~30 min)
Medicare ASP+6%
$20.546
per mg, Q2 2026 · $2,054.60/100 mg
HCPCS descriptor
J3032 — "Injection, eptinezumab-jjmr, 1 mg" Permanent 4/1/21
Adult dosing options
100 mg IV q3 months (recommended starting dose) or 300 mg IV q3 months (some patients may benefit). 4 infusions/year.
Vial
100 mg / 1 mL (100 mg/mL) single-dose vial — must be diluted in 100 mL 0.9% NaCl before infusion
Route
IV infusion over approximately 30 minutes — NOT an injection. Diluted and infused via gravity or pump.
NDC (carton)
00187-1530-91 (10) / 00187-1530-91 (11) — Lundbeck labeler code 00187
Manufacturer
H. Lundbeck A/S (US affiliate Lundbeck Inc.) — Vyepti Connect 1-833-389-3784
Premedication
Not routinely required. Anaphylaxis precautions advised — epinephrine availability + observation period.
Boxed warning
None. W&P: hypersensitivity reactions (urticaria, angioedema, anaphylaxis), nasopharyngitis, fatigue.
FDA approval
February 21, 2020 (BLA 761119); label most recently revised 2025.
ℹ️
Vyepti is the only IV anti-CGRP for migraine prevention. The other three FDA-approved anti-CGRP monoclonal antibodies — Aimovig (erenumab-aooe, Amgen/Novartis), Ajovy (fremanezumab-vfrm, Teva), and Emgality (galcanezumab-gnlm, Lilly) — are subcutaneous self-injected pens/syringes and bill under Medicare Part D / pharmacy benefit. Vyepti, because it requires provider IV administration, bills under Medicare Part B / medical benefit. Major implication: Vyepti reimbursement, prior auth pathways, and patient out-of-pocket calculations are fundamentally different from the SC anti-CGRPs. See comparison table.
⚠️
Step therapy is the norm for commercial PA. Most major payers (UHC, Aetna, BCBS) require documented failure, intolerance, or contraindication to (1) at least two oral migraine prophylactic agents (e.g., topiramate, propranolol, amitriptyline, divalproex) and (2) at least one SC anti-CGRP (Aimovig, Ajovy, or Emgality). Document the trial duration (typically 8 weeks per oral agent) and reason for discontinuation in the PA submission. See payer policy snapshot.
Phase 1 Identify what you're billing Confirm IV (Vyepti, Part B) vs SC anti-CGRPs (Aimovig/Ajovy/Emgality, Part D) before doing anything else.

Vyepti (IV) vs. Aimovig / Ajovy / Emgality (SC) FDA verified May 2026

All four are anti-CGRP monoclonal antibodies for migraine prevention — but the billing pathways are completely different.

The four FDA-approved anti-CGRP monoclonal antibodies for migraine prevention divide cleanly into two billing camps. Vyepti is the only one administered intravenously by a healthcare provider, which puts it under the medical benefit (Part B for Medicare). The other three are subcutaneous self-injection devices (autoinjector pens or prefilled syringes), which puts them under the pharmacy benefit (Part D for Medicare). This single distinction drives every downstream billing and reimbursement difference.

Side-by-side comparison of Vyepti IV and the three subcutaneous anti-CGRP migraine preventives.
VyeptiAimovigAjovyEmgality
Genericeptinezumab-jjmrerenumab-aooefremanezumab-vfrmgalcanezumab-gnlm
ManufacturerLundbeckAmgen / NovartisTevaEli Lilly
RouteIV infusionSC self-injectSC self-injectSC self-inject
HCPCSJ3032J3031 (in-office) / Part D pharmacyJ3245 (in-office) / Part D pharmacyJ3590 / Part D pharmacy
BenefitMedical (Part B)Pharmacy (Part D)Pharmacy (Part D)Pharmacy (Part D)
Scheduleq3 months (4/yr)Monthly (12/yr)Monthly OR quarterlyMonthly (12/yr) + 240 mg loading
Admin time~30 min IV15 sec SC15 sec SC15 sec SC
Admin CPT96365 (non-chemo IV)None (pt self-administers)None (pt self-administers)None (pt self-administers)
Standard dose100 mg or 300 mg70 mg or 140 mg225 mg monthly OR 675 mg quarterly120 mg (after 240 mg load)
Adherence advantage4 visits/yr12 self-injections12 monthly OR 4 quarterly12 self-injections
Why Vyepti's billing pathway matters: Because Vyepti requires provider administration, it bills under the medical benefit — CMS-1500 / 837P, J3032 + 96365, with prior auth through the medical drug review pathway. The SC anti-CGRPs go through specialty pharmacy: prescription, pharmacy benefit PA, patient pays pharmacy copay/coinsurance, drug ships to patient or office. The two pathways have different deductibles, copay structures, and patient-assistance program rules.
Adherence is Vyepti's clinical-economic story. Real-world adherence to monthly SC anti-CGRPs is approximately 50–60% at 12 months. Vyepti's 4-visit-per-year cadence with provider administration materially improves adherence, which payers increasingly factor into total cost-of-care calculations even though Vyepti's per-dose acquisition cost is higher.

Dosing & unit math FDA label 2025

From the FDA prescribing information (BLA 761119), label revised 2025.

Adult dosing

  • 100 mg IV every 3 months — recommended starting dose, FDA-approved for both episodic and chronic migraine prevention
  • 300 mg IV every 3 months — some patients may benefit from this higher dose; per FDA label, may be considered for patients with chronic migraine or inadequate response to 100 mg
  • Both doses are administered every 3 months — 4 infusions per year
  • 1 mg = 1 unit — bill 100 or 300 units per dose
  • No loading dose required
  • No weight-based or renal/hepatic dose adjustment in adults

Preparation & administration

  • Vyepti supplied as 100 mg / 1 mL single-dose vial (100 mg/mL)
  • Must be diluted in 100 mL of 0.9% sodium chloride for IV infusion (no other diluent)
  • For 100 mg dose: withdraw 1 mL Vyepti, inject into 100 mL NaCl bag (final volume ~101 mL)
  • For 300 mg dose: withdraw 3 mL Vyepti from three vials, inject into 100 mL NaCl bag (final volume ~103 mL)
  • Infuse over approximately 30 minutes via gravity or pump
  • Do NOT administer as IV push or as undiluted SC/IM injection
  • Discard any unused portion of the single-dose vial

Worked example — first-year billing for a 100 mg q3-month dose

# 4 infusions per year (q3 months)
Drug units billed per dose: 100 (J3032)
HCPCS: J3032 · Modifier: JZ · Vials: 1 × 100 mg single-dose
Admin: 96365 (~30-min therapeutic IV, non-chemo)

# Year-1 totals
Total infusions: 4
Total drug units billed: 400 (4 × 100)
Total drug cost (Q2 2026 ASP+6%): ~$8,218 before sequestration
Plus 4 × 96365 admin

Worked example — 300 mg q3-month dose

# 4 infusions per year (q3 months)
Drug units billed per dose: 300 (J3032)
HCPCS: J3032 · Modifier: JZ · Vials: 3 × 100 mg single-dose
Admin: 96365 (~30-min therapeutic IV, non-chemo)

# Year-1 totals
Total infusions: 4
Total drug units billed: 1,200 (4 × 300)
Total drug cost (Q2 2026 ASP+6%): ~$24,655 before sequestration

No premedication routinely required

Per the FDA label, premedication with corticosteroids or antihistamines is NOT routinely required for Vyepti. However, hypersensitivity reactions including urticaria, angioedema, and anaphylaxis have been reported. Anaphylaxis precautions are advised: ensure epinephrine is immediately available, observe the patient during and for an appropriate period after the infusion, and be prepared to manage acute hypersensitivity. Most reactions occur during or shortly after the infusion.

NDC reference FDA NDC Directory verified May 2026

NDC (10/11-digit)PackageUse
0187-1530-91 / 00187-1530-91 100 mg / 1 mL single-dose vial — 1 vial per carton Standard 100 mg adult dose (1 vial) or 300 mg adult dose (3 vials)
Use carton-level NDC, not vial-level. Payers expect the carton NDC on the claim form with N4 qualifier. Vial-level NDC will trigger denial. The 100 mg dose uses one carton; the 300 mg dose uses three cartons.
Lundbeck labeler code: 00187. Vyepti was approved February 21, 2020 and launched in 2020. It is the first and to date only IV anti-CGRP monoclonal antibody for migraine prevention.
Phase 2 Code the claim Use therapeutic IV admin codes (96365/96366), NOT chemo admin (96413/96415).

Administration codes CPT verified May 2026

Vyepti is a non-chemotherapy biologic. Use 96365 (and 96366 only if needed). Do NOT use 96413/96415.

CodeDescriptionWhen to use
96365 Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); initial, up to 1 hour Primary code for Vyepti. Standard 30-min infusion fits within the 1-hour window.
96366 Intravenous infusion, for therapy, prophylaxis, or diagnosis; each additional hour Add only if the total infusion exceeds 1 hour. Uncommon for Vyepti.
96413 / 96415 Chemotherapy administration, IV infusion (initial / each additional hour) NOT appropriate. Vyepti is a non-chemotherapy biologic. Chemo admin codes will trigger denial or recoupment.
96372 Therapeutic, prophylactic, or diagnostic injection (SC or IM) NOT appropriate. Vyepti is an IV infusion, not an injection. The drug must be diluted and infused.
Why 96365 (not 96413): CPT chemotherapy administration codes (96409–96425) are reserved for cytotoxic chemotherapy and certain complex monoclonal antibody oncology infusions. Eptinezumab is a non-cytotoxic biologic for migraine prevention — therapeutic IV infusion (96365) is the correct code. Billing 96413 will trigger payer recoupment.
Do not bill Vyepti as an injection (96372). The drug cannot be administered SC or IM and must be diluted in 100 mL of 0.9% NaCl for IV infusion. Billing 96372 mismatches the route documented in the medical record and will trigger denial.

Modifiers CMS verified May 2026

JZ — required on virtually every Vyepti claim

Effective July 1, 2023, CMS requires the JZ modifier on all single-dose container claims when no drug is discarded. The Vyepti 100 mg dose uses one 100 mg single-dose vial with zero waste; the 300 mg dose uses three vials with zero waste. JZ applies to virtually every Vyepti claim.

JW — only if partial-vial waste occurs

JW reports the discarded portion of a single-dose vial. For Vyepti, JW would only apply in rare scenarios where a partial vial is discarded (e.g., a clinical-trial protocol or off-label weight-based pediatric scenario). For the standard 100 mg or 300 mg adult flat doses, there is no waste and JZ applies. One of JZ or JW must be on every J3032 claim.

Modifier 25 — same-day E/M

Use modifier 25 on the E/M code when a significant, separately identifiable evaluation and management service is performed on the same day as the infusion (e.g., headache neurology follow-up before infusion). Routine pre-infusion clinical assessment is bundled.

340B modifiers (JG, TB)

For 340B-acquired Vyepti, follow your MAC's current 340B modifier policy. Headache neurology clinics within 340B-eligible health systems should track 340B vs non-340B inventory carefully.

ICD-10-CM by indication FY2026 verified May 2026

Vyepti is FDA-approved for preventive treatment of migraine in adults (episodic OR chronic). Use the most specific G43 code supported by encounter documentation.

ICD-10DescriptionNotes
G43.001 / G43.009Migraine without aura, not intractable, with / without status migrainosusEpisodic migraine without aura
G43.011 / G43.019Migraine without aura, intractable, with / without status migrainosusEpisodic intractable
G43.101 / G43.109Migraine with aura, not intractable, with / without status migrainosusEpisodic migraine with aura
G43.111 / G43.119Migraine with aura, intractable, with / without status migrainosusEpisodic intractable with aura
G43.701 / G43.709Chronic migraine without aura, not intractable, with / without status migrainosusChronic migraine (≥15 headache days/month)
G43.711 / G43.719Chronic migraine without aura, intractable, with / without status migrainosusChronic intractable
G43.801 / G43.809Other migraine, not intractable, with / without statusLess common subtypes
G43.811 / G43.819Other migraine, intractable, with / without statusLess common subtypes intractable
G43.901 / G43.909Migraine, unspecified, not intractable, with / without statusUse only if specificity not documented
G43.911 / G43.919Migraine, unspecified, intractable, with / without statusUse only if specificity not documented
Distinguish chronic from episodic in documentation. Chronic migraine (G43.7x, ≥15 headache days/month for >3 months, with at least 8 days having migraine features) often requires different PA criteria from episodic migraine (G43.0x, G43.1x, <15 headache days/month). Many payers have separate medical-necessity criteria for chronic vs episodic, and chronic migraine may have a higher bar for prior failed therapies.
Document migraine days per month and prior therapies. Most payer PA forms require baseline monthly migraine days (MMD) or monthly headache days (MHD), prior preventive therapies tried, duration of each trial, and reason for discontinuation. Vyepti's clinical trial population (PROMISE-1 and PROMISE-2) included patients with 4–14 MMD (episodic) and ≥15 MHD with ≥8 migraine days (chronic).

Site of care & place of service Verified May 2026

Vyepti's 30-minute infusion fits cleanly into multiple sites of care. Document POS appropriately on the claim form — Vyepti can be administered in physician offices (most common), ambulatory infusion centers, hospital outpatient departments, and via home infusion through some vendors (Coram, SDS, Option Care) where the payer permits. UnitedHealthcare and Aetna run site-of-care UM that disfavors HOPD for non-emergency biologic infusions.

SettingPOSClaim formPayer steering
Physician office (neurology / headache clinic)11CMS-1500 / 837PPreferred by commercial UM
Ambulatory infusion center49CMS-1500 / 837PPreferred by commercial UM
Hospital outpatient (on-campus)22UB-04 / 837IDisfavored for routine maintenance infusions
Hospital outpatient (off-campus PBD)19UB-04 / 837IDisfavored for routine maintenance infusions
Patient home (home infusion)12CMS-1500 + S9329 home infusion codePossible via Coram/SDS/Option Care if payer permits
Site-of-care opportunity: Vyepti's 30-minute infusion + low monitoring requirement (no premedication, no boxed warning) makes it well-suited to office-based administration. Headache neurology practices and ambulatory infusion centers can capture the full medical-benefit revenue stream rather than referring patients to HOPD. Some payers also permit home infusion via specialty home-infusion vendors — check Vyepti Connect for vendor referrals.

Claim form field mapping Lundbeck Vyepti Connect 2026

Standard CMS-1500 / 837P fields. UB-04 / 837I if billed under HOPD.

InformationCMS-1500 boxNotes
NPI17bRendering provider (often headache neurologist)
NDC qualifier + 11-digit NDC + UoM + qty24A shaded areaN4 00187153091 ML 1 (100 mg dose) / N4 00187153091 ML 3 (300 mg dose)
HCPCS J3032 + JZ24D (drug line)JZ on virtually every claim (no waste)
Drug units24G100 (for 100 mg dose) or 300 (for 300 mg dose)
CPT 96365 (admin line)24D (admin line)30-min infusion fits within 1-hour window
ICD-1021Indication-specific G43.x (chronic vs episodic)
PA number23Required by all major commercial payers
Prior therapies attestationAttached PA documentationDocument failed oral prophylactics + SC anti-CGRP trial
Phase 3 Get paid Step therapy from oral prophylactics + SC anti-CGRP is the dominant payer requirement.

Payer policy snapshot + step therapy Reviewed May 2026

Most commercial payers require documented failure or intolerance to oral prophylactics AND at least one SC anti-CGRP before approving Vyepti.

PayerPA?Step therapy requirementSite-of-care UM
UnitedHealthcare
Commercial Medical Drug Policy
Yes Failure / intolerance / contraindication to ≥2 oral preventives (different classes) AND ≥1 SC anti-CGRP (Aimovig, Ajovy, or Emgality), each with ≥8-week trial documented Yes — SOC steering away from HOPD
Aetna
CPB Migraine Therapies
Yes Documented failure / intolerance to ≥2 oral preventives + trial of SC anti-CGRP. Chronic migraine may have additional onabotulinumtoxinA (Botox) trial requirement on some plans. Yes (separate Site-of-Care policy)
BCBS plans
Vary by plan
Yes Generally aligned with commercial step-therapy norm (oral prophylactics + SC anti-CGRP); some plans require documented chronic migraine for 300 mg dose Plan-specific
Medicare Part B (FFS)
No NCD; MAC LCDs apply
Generally no PA in FFS No federal step therapy for FFS Medicare; covers J3032 for FDA-approved indication with appropriate ICD-10 N/A in FFS; MA plans may impose
Medicare Advantage Yes (most plans) MA plans may impose step therapy under CMS Part B step-therapy authority granted in 2018; verify plan-specific criteria Plan-specific

Documentation checklist for PA

  • Diagnosis: ICD-10 G43.x with chronic vs episodic distinction documented
  • Baseline migraine frequency: Monthly migraine days (MMD) and / or monthly headache days (MHD) over ≥3 months
  • Oral preventive trials: ≥2 agents from different classes (e.g., topiramate, propranolol, amitriptyline, divalproex), ≥8 weeks each, with reason for discontinuation (lack of efficacy, intolerable AE, contraindication)
  • SC anti-CGRP trial: ≥1 of Aimovig / Ajovy / Emgality with documented adequate trial (typically ≥3 monthly doses or 1 quarterly dose) and reason for discontinuation
  • Prescriber: Many payers require a neurologist or headache specialist; check plan
  • Site of care attestation: Documenting POS 11 / 49 (office or AIC) facilitates approval
AHS guideline alignment: The American Headache Society 2024 consensus statement supports anti-CGRP mAbs (including IV eptinezumab) as first-line preventive options for adults with migraine, without requiring step therapy through older oral preventives in clinical practice. Payers, however, continue to enforce step therapy as a cost-control measure regardless of guideline language.

Medicare reimbursement CMS Q2 2026 (live)

Quarterly ASP from CMS Part B Drug Pricing File. Refreshes automatically each quarter.

Q2 2026 payment snapshot — J3032

Effective April 1 – June 30, 2026 · Based on 4Q25 ASP submissions

ASP + 6%
$20.546
per mg / per unit
100 mg dose (q3 mo)
$2,054.60
100 units × ASP+6%
300 mg dose (q3 mo)
$6,163.80
300 units × ASP+6%
Annualized cost: 100 mg q3 months × 4 doses = ~$8,218/year (Medicare ASP+6%). 300 mg q3 months × 4 doses = ~$24,655/year. After ~2% sequestration: ~$8,000 and ~$24,000 actual paid, respectively. Significantly less than oncology biologics but materially more than oral migraine prophylactics (often <$500/year generic).

Coverage

No NCD specific to eptinezumab. Coverage falls under MAC LCDs for biologics + the generic Part B physician-administered drug framework. All MACs cover J3032 for the FDA-approved indication (preventive treatment of migraine in adults) with appropriate ICD-10 documentation. Medicare FFS does not impose step therapy at the federal level, but Medicare Advantage plans may.

Code history

  • Pre-permanent code (Feb 2020 – Mar 2021): billed under unclassified J3490 / J3590 with NDC + dose documentation
  • J3032 — permanent code, effective April 1, 2021

Patient assistance — Vyepti Connect Lundbeck verified May 2026

  • Vyepti Connect: 1-833-389-3784 / vyepti.com — benefits investigation, prior authorization assistance, appeal support, site-of-care navigation
  • Vyepti Co-pay Card: commercial copay support — eligible commercially insured patients pay $0 per infusion, up to $20,000 per calendar year (excludes Medicare, Medicaid, federal program patients)
  • Vyepti Patient Assistance Program (PAP): free product for uninsured / underinsured patients meeting income requirements
  • Foundations: for Medicare patients, refer to PAN, HealthWell, Good Days for migraine / neurology funds — verify open funds quarterly
  • Web: vyepti.com · HCP portal: vyeptihcp.com
Need to model what a specific patient will actually pay after copay assistance, deductible, coinsurance, and OOP max? Run a CareCost Estimate — J3032 pre-loaded.
Phase 4 Fix problems Step-therapy documentation gaps, wrong admin code, and chronic-vs-episodic confusion are the top three.

Common denials & how to fix them

Denial reasonCommon causeFix
Step therapy not satisfiedPA submitted without documented oral prophylactic and / or SC anti-CGRP trialsResubmit with full prior-therapy documentation: agents, doses, durations (≥8 weeks each), reasons for discontinuation. Include SC anti-CGRP trial history (≥3 months).
Wrong admin code (96413)Chemo IV billed instead of therapeutic IVResubmit with 96365. Vyepti is a non-chemotherapy biologic and does NOT qualify for 96413/96415.
Wrong admin code (96372)Injection code used for an infusionResubmit with 96365. Vyepti must be diluted and infused — it is not an SC/IM injection.
JZ missing on claimSingle-dose vial claim without JZ modifierResubmit with JZ. Required since 7/1/2023 on every single-dose vial claim with no waste.
Wrong NDC format (vial-level)Vial NDC submitted instead of carton NDCUse carton NDC 00187-1530-91 with N4 qualifier. ML unit of measure, qty 1 (100 mg dose) or 3 (300 mg dose).
Site of care (HOPD)HOPD administration on commercial plan with site-of-care UMMove to office (POS 11), AIC (POS 49), or home infusion (POS 12). Submit medical necessity letter if HOPD truly required.
Chronic vs episodic mismatchG43.0x / G43.1x submitted but PA criteria require chronic migraine (G43.7x)Verify ICD-10 matches the PA criteria for the requested dose. 300 mg dose may have stricter chronic-migraine documentation requirements on some plans.
Vyepti billed under Part DPharmacy benefit submission for an IV provider-administered drugVyepti bills Part B medical benefit, not Part D pharmacy. Resubmit through medical drug pathway with CMS-1500.
Aimovig / Ajovy / Emgality billed under J3032SC anti-CGRP miscoded as VyeptiAimovig = J3031 (in-office) or Part D; Ajovy = J3245 (in-office) or Part D; Emgality = J3590 / Part D. Vyepti is the only IV anti-CGRP and the only one billing under J3032.

Frequently asked questions

What is the HCPCS code for Vyepti?

Vyepti (eptinezumab-jjmr IV) is billed under HCPCS J3032 — "Injection, eptinezumab-jjmr, 1 mg." Each milligram equals one billable unit, so the standard 100 mg q3-month dose is billed as 100 units, and the 300 mg dose as 300 units. J3032 has been a permanent code effective April 1, 2021.

How many units do I bill for a Vyepti dose?

Bill 100 units of J3032 per 100 mg dose (one 100 mg single-dose vial) and 300 units per 300 mg dose (three 100 mg vials). Both doses are administered every 3 months — 4 infusions per year. Year-1 totals: 400 units (100 mg dose) or 1,200 units (300 mg dose).

What administration CPT do I use for Vyepti?

CPT 96365 — "Intravenous infusion, for therapy, prophylaxis, or diagnosis (specify substance or drug); initial, up to 1 hour" is the primary code. Vyepti's standard infusion is approximately 30 minutes, fitting within the 1-hour 96365 window. Add 96366 ("each additional hour") only if the infusion extends beyond 1 hour. Do NOT bill 96413/96415 — those are chemotherapy administration codes and are inappropriate for eptinezumab. Do NOT bill 96372 — Vyepti is not an injection; it must be diluted and infused.

Do I bill JZ or JW for Vyepti?

Bill JZ on virtually every Vyepti claim. The 100 mg dose uses one 100 mg single-dose vial with zero waste; the 300 mg dose uses three vials with zero waste. JW would only apply in rare partial-vial-discard scenarios. One of JZ or JW must be on every J3032 claim per CMS's July 2023 single-dose container policy.

What is the Medicare reimbursement for J3032?

For Q2 2026, the Medicare Part B payment limit for J3032 is $20.546 per mg (ASP + 6%). The 100 mg q3-month dose reimburses at approximately $2,054.60 per infusion; the 300 mg dose at approximately $6,163.80. Annualized cost (Medicare ASP+6%): ~$8,218 (100 mg dose) or ~$24,655 (300 mg dose). Sequestration (~2%) reduces actual paid to roughly ASP + 4.3%.

Does Vyepti require step therapy?

Yes for most commercial payers. UnitedHealthcare, Aetna, and most major BCBS plans require documented failure, intolerance, or contraindication to (1) at least two oral migraine prophylactic agents from different classes (e.g., topiramate, propranolol, amitriptyline, divalproex) and (2) at least one subcutaneous anti-CGRP (Aimovig, Ajovy, or Emgality). Documentation of trial duration (typically ≥8 weeks per oral agent), monthly migraine days, and reason for discontinuation is required. Medicare Part B FFS does not impose step therapy at the federal level for J3032, but Medicare Advantage plans may.

What is the difference between Vyepti and the other anti-CGRP migraine drugs?

Vyepti (eptinezumab-jjmr, Lundbeck, J3032) is the only intravenous anti-CGRP for migraine prevention — administered every 3 months in a clinical setting (4 visits per year). The three subcutaneous anti-CGRPs are: Aimovig (erenumab-aooe, Amgen/Novartis) — monthly self-injection; Ajovy (fremanezumab-vfrm, Teva) — monthly OR quarterly self-injection; Emgality (galcanezumab-gnlm, Lilly) — monthly self-injection. The SC drugs bill under Medicare Part D / pharmacy benefit; Vyepti bills under Part B / medical benefit because it requires provider administration. Vyepti's primary advantage is adherence (4 in-office visits vs 12 monthly self-injections) and faster onset of effect.

Is premedication required for Vyepti?

Premedication is NOT routinely required per the FDA label. However, hypersensitivity reactions including urticaria, angioedema, and anaphylaxis have been reported. Anaphylaxis precautions are advised: epinephrine should be available, the patient should be observed during and for an appropriate period after infusion, and providers should be prepared to manage acute hypersensitivity. There is no boxed warning on the Vyepti label.

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

Source documents

  1. Vyepti HCP — coding & coverage information
    Lundbeck Vyepti HCP portal: dosing, administration, billing
  2. DailyMed — VYEPTI (eptinezumab-jjmr) Prescribing Information
    FDA-approved label, BLA 761119, revised 2025
  3. FDA Vyepti label PDF (initial approval, February 21, 2020)
  4. CMS — Medicare Part B Drug ASP Pricing File
    Q2 2026 quarterly file, effective April 1 – June 30, 2026
  5. American Headache Society — preventive treatment consensus statement
    2024 AHS consensus on anti-CGRP mAbs as first-line preventive options
  6. UnitedHealthcare — Commercial Medical Drug Policies (eptinezumab)
  7. Aetna — CPB on Migraine Therapies (anti-CGRP mAbs)
  8. Vyepti Co-pay Card — Lundbeck commercial copay program
    $0 per infusion up to $20,000/year for eligible commercially insured patients
  9. Vyepti Connect — 1-833-389-3784 patient & provider support
  10. FDA National Drug Code Directory

About this page

We maintain this page as a living reference. Medicare ASP pricing is bound to our underlying CareCost data layer and refreshes automatically when CMS publishes new quarterly files. Coding and policy content is reviewed at least quarterly and updated whenever a source document 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 policies (UHC, Aetna, BCBS)Semi-annualManual review against published payer policy documents.
HCPCS / CPT / modifier rulesAnnualReviewed against CMS HCPCS quarterly files and AMA CPT releases.
NDC, dosing, FDA label, indicationEvent-drivenTied to manufacturer document version + FDA label revision date.

Reviewer

Pending SME review. This page is staff-authored from primary sources (FDA, CMS, manufacturer, payer documents — all linked above). Editorial review in progress. Until that review is complete, treat this as a draft reference and verify each cited source for high-stakes claims.

Change log

  • — Initial publication. ASP data: Q2 2026. Manufacturer source: Lundbeck Vyepti HCP / Vyepti Connect 2026. FDA label: 2025 revision (BLA 761119). Indication: preventive treatment of migraine in adults (episodic + chronic). Sister SC anti-CGRPs (Aimovig, Ajovy, Emgality) referenced for benefit-design comparison.

Methodology

Every claim on this page is sourced inline. Pricing reflects the current CMS Part B Drug ASP Pricing File. Payer policies are read directly from each payer's published medical/pharmacy policy documents. Indication and dosing are verified against the current FDA label revision. We do not paraphrase from billing-software vendor blogs.

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