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Prescription medicine

Marstacimab Brand names: Hympavzi

Marstacimab (Hympavzi) is a prescription medicine. No generic is listed in FDA's NDC Directory.

  • No generic listed

Check it at the source: the marstacimab FDA label on DailyMed (effective June 22, 2026); every marstacimab label on DailyMed.

Highlights of the record

FDA label of June 22, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

HYMPAVZI is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with:

hemophilia A (congenital factor VIII deficiency) with or without factor VIII inhibitors, or

hemophilia B (congenital factor IX deficiency) with or without factor IX inhibitors.

Forms and strengths

  • 75 mg/.5ml
  • 150 mg/ml

Injection (solution).

On the market

Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
84 through July 30, 2026

What is marstacimab used for?

From the label: indications and usage

HYMPAVZI is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients 6 years of age and older with:

hemophilia A (congenital factor VIII deficiency) with or without factor VIII inhibitors, or

hemophilia B (congenital factor IX deficiency) with or without factor IX inhibitors. […]

Source: FDA drug label (HYMPAVZI), Pfizer Laboratories Div Pfizer Inc, effective June 22, 2026 (SPL set a2cc631e-13a6-40c2-acf9-065ccedfb90a), via openFDA; the full label on DailyMed

Is there a generic for marstacimab (Hympavzi)?

No generic marstacimab is approved (Drugs@FDA, October 8, 2026).

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do FAERS reports show for marstacimab?

The FDA Adverse Event Reporting System holds 84 reports that list marstacimab among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 1 are coded as a death and 15 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

The most reported reactions

  • Haemarthrosis15
  • Haemorrhage (named in the label)12
  • Device Defective6
  • Drug Dose Omission By Device (a use or a product term, not a reaction)6
  • Contusion5
  • Arthralgia (named in the label)4
  • Device Failure4
  • Drug Ineffective (a use or a product term, not a reaction)4

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Marstacimab side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other