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Molecule

Ansuvimab

Zaire Ebolavirus Glycoprotein-directed Antibody
Available on requestBiologicOrphanCold chainImmunoglobulins
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Ansuvimab is a zaire ebolavirus glycoprotein-directed antibody indicated for the treatment of infection caused by Orthoebolavirus zairense (formerly Zaire ebolavirus) in adult and pediatric patients, among other approved uses. MedsAcross supplies Ansuvimab for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Zaire Ebolavirus Glycoprotein-directed Antibody, Zaire Ebolavirus Glycoprotein-directed Antibody Interactions
ATC classification
J06BD04 Ansuvimab · Immunoglobulin therapy, subgroup J06BD
US FDA first approval
21 December 2020
EU status
Not recorded
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Powder for injection
Biologic
Yes
Identifiers
UNII TG8IQ19NG2Q59554781

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

EBANGA is indicated for the treatment of infection caused by Orthoebolavirus zairense (formerly Zaire ebolavirus) in adult and pediatric patients, including neonates born to a mother who is RT-PCR positive for Orthoebolavirus zairense infection. EBANGA (ansuvimab-zykl) is an Orthoebolavirus zairense glycoprotein (EBOV GP)-directed human monoclonal antibody indicated for the treatment of infection caused by Orthoebolavirus zairense in adult and pediatric patients, including neonates born to a mother who is RT-PCR positive for Orthoebolavirus zairense infection. Limitation of Use The efficacy of EBANGA has not been established for other species of the Orthoebolavirus and Orthomarburgvirus genera. Orthoebolavirus zairense can change over time, and factors such as emergence of resistance or changes in viral virulence could diminish the clinical benefit of antiviral drugs.

Source: US FDA prescribing information

How it works

Ansuvimab-zykl is a recombinant human monoclonal antibody with antiviral activity against Orthoebolavirus zairense.

Source: US FDA prescribing information

Dosing overview

The recommended dose of EBANGA for adult and pediatric patients is 50 mg/kg reconstituted, further diluted, and administered as a single intravenous infusion over 60 minutes. See Full Prescribing Information for instructions on preparation, dilution and administration of EBANGA injection.

Source: US FDA prescribing information

Warnings and precautions

Hypersensitivity Reactions Including Infusion-Associated Events: Hypersensitivity reactions including infusion-associated events have been reported with EBANGA. These may include acute, life- threatening reactions during and after the infusion. Monitor patients and in the case of severe or life-threatening hypersensitivity reactions, discontinue the administration of EBANGA immediately and administer appropriate emergency care.

Source: US FDA prescribing information

Side effects

The following clinically significant adverse reactions are described elsewhere in the labeling: Hypersensitivity Reactions Including Infusion-Associated Events The most frequently reported adverse events (≥ 5%) after administration of EBANGA were pyrexia, tachycardia, diarrhea, vomiting, hypotension, tachypnea, and chills.

Source: US FDA prescribing information

Interactions

Interaction with live vaccine indicated for prevention of Orthoebolavirus zairense infection: No vaccine interaction studies have been performed. EBANGA may reduce the efficacy of the live vaccine. The interval between administration of EBANGA therapy and live vaccination should be in accordance with current vaccination guidelines.

Source: US FDA prescribing information

Storage

Store refrigerated at 2ºC to 8ºC (36ºF to 46ºF) in the original carton to protect from light. Do not freeze. Do not shake. Prior to reconstitution, allow EBANGA vial(s) to reach ambient temperature (15°C to 27°C [59°F to 81°F]) for approximately 20 minutes. If for any reason reconstitution cannot proceed immediately upon reaching ambient temperature, vials that have NOT been reconstituted may be kept at ambient temperature, protected from light, for no more than 24 hours.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

1 presentations of Ansuvimab, sorted by availability.

MedicineManufacturerRegisterAvailability
Ebanga 400 mg/8 mL powder for injectionIntravenous Cold chainEmergent BioDefense Operations LansingUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 21 December 2020Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Ansuvimab available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Ansuvimab and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Ansuvimab have?

The catalogue lists 1 brand names for Ansuvimab, including Ebanga.

Is Ansuvimab approved by the US FDA?

Yes. The US FDA first approved Ansuvimab on 21 December 2020, according to Drugs@FDA.

Does Ansuvimab need cold chain shipping?

At least one listed presentation of Ansuvimab must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

Which ATC class is Ansuvimab in?

Ansuvimab is classified under ATC code J06BD04 (Ansuvimab).

References

  1. Ebanga prescribing information (Emergent BioDefense Operations Lansing). U.S. National Library of Medicine, DailyMed. Retrieved 13 August 2026

Request Ansuvimab for export supply

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