Monjuvi is given by a doctor or nurse and billed by the clinic, not a pharmacy. Your care team and your insurance decide which product you get, so ask them what you’d pay.

How do you pay?

How to pay the least

Given by your care team

Billed by the clinic

Monjuvi is given by a doctor or nurse, not picked up at a pharmacy.

  1. Ask your care team or your plan what you’d pay before your visit.

Compare every option

Question
Brand nameMonjuvi
Authorized generictafasitamab-cxix
Regular generictafasitamab-cxix
What you’d pay
Cash priceAsk the pharmacy
Not soldThere isn’t one
Not soldAsk the pharmacy
Same as Monjuvi?
The original
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–

Brand nameThe maker’s card

IncyteCARES Savings Program for MONJUVI

Savings card from Incyte

No insuranceNeeds insuranceNo cash price listed.
Insurance · as little as $15 a prescription

Sign up on incytecares.com 

Or call 1-855-452-5234.

In the maker’s words

“Eligible patients can receive MONJUVI for as little as $15, subject to certain limits…”

From the maker’s offer on incytecares.com, checked November 2, 2026. Co-pay cards can’t be used with Medicare (including Medicare Advantage), Medicaid, TRICARE or VA.

Authorized genericNot sold

There isn’t one. An authorized generic is Monjuvi itself, from the same company, sold without the brand name, and usually for less. For now Monjuvi is the only choice; its maker’s savings card can lower what you pay.

See the brand name →

Regular genericNot sold

Monjuvi is a biologic. Biologics don’t have generics, but some have biosimilars or an unbranded version from the same maker. Ask your pharmacist or prescriber whether one is sold. Generics usually come once the brand’s patents and exclusivity end. Until then, the maker’s savings card is the way to pay less.

See the brand name →

What it’s used for

What the FDA label says

MONJUVI is a CD19-directed cytolytic antibody indicated:

  • in combination with lenalidomide for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL arising from low grade lymphoma, and who are not eligible for autologous stem cell transplant (ASCT). This indication is approved under accelerated approval based on overall response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).
  • in combination with lenalidomide and rituximab for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL).

Limitations of Use:

MONJUVI is not indicated and is not recommended for the treatment of patients with relapsed or refractory marginal zone lymphoma outside of controlled clinical trials.

Source: the FDA label for Monjuvi (Incyte Corporation), June 23, 2025. Full label on DailyMed 

Good to know