Skip to content
MedsAcross

Fixed-dose combination

Netupitant and Palonosetron

Also known as netupitant, palonosetron
Available on requestCold chainGastroenterology
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Netupitant and Palonosetron is a fixed-dose combination of a serotonin-3 receptor antagonist and a substance P/neurokinin-1 receptor antagonist. It is available as capsules for oral use. MedsAcross supplies Netupitant and Palonosetron 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
Serotonin-3 Receptor Antagonist, Substance P/Neurokinin-1 Receptor Antagonist, Breast Cancer Resistance Protein Inhibitors, Cytochrome P450 3A4 Inhibitors, Neurokinin 1 Antagonists, P-Glycoprotein Inhibitors, Serotonin 3 Receptor Antagonists
ATC classification
A04AA Anti-nausea and anti-vomiting medicines, subgroup A04A, subgroup A04AA · Anti-nausea and anti-vomiting medicines, subgroup A04A
US FDA first approval
10 October 2014
EU status
Authorised
Orphan designation
No
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Capsule
Fixed-dose combination of
Netupitant, Palonosetron
Identifiers
RxCUI 1552342Q19598140

Clinical information

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

Uses

AKYNZEO capsules is indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy. AKYNZEO capsules is a combination of palonosetron and netupitant: palonosetron prevents nausea and vomiting during the acute phase and netupitant prevents nausea and vomiting during both the acute and delayed phase after cancer chemotherapy. AKYNZEO for injection and AKYNZEO injection are indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy.

Source: US FDA prescribing information

How it works

Netupitant is a selective antagonist of human substance P/neurokinin 1 (NK-1) receptors. Palonosetron is a 5-HT 3 receptor antagonist with a strong binding affinity for this receptor and little or no affinity for other receptors. Cancer chemotherapy may be associated with a high incidence of nausea and vomiting, particularly when certain agents, such as cisplatin, are used. 5-HT 3 receptors are located on the nerve terminals of the vagus in the periphery and centrally in the chemoreceptor trigger zone of the area postrema. Chemotherapeutic agents produce nausea and vomiting by stimulating the release of serotonin from the enterochromaffin cells of the small intestine. Serotonin then activates 5-HT 3 receptors located on vagal afferents to initiate the vomiting reflex.

Source: US FDA prescribing information

Dosing overview

Recommended Dosage AKYNZEO capsules: The recommended dosage is one AKYNZEO capsule administered 1 hour prior to the start of chemotherapy, with or without food. Preparation and Administration AKYNZEO injection is supplied either as a Ready-to-Use (with hanger) vial or a To-be-Diluted vial. AKYNZEO for injection requires dilution prior to administration. See full prescribing information for information on preparation, administration, and incompatibilities for each product.

Source: US FDA prescribing information

Warnings and precautions

Hypersensitivity reactions, including anaphylaxis, have been reported in patients receiving palonosetron, one of the components of AKYNZEO, with or without known hypersensitivity to other 5-HT 3 receptor antagonists. Serotonin syndrome has been reported with 5-HT 3 receptor antagonists alone but particularly with concomitant use of serotonergic drugs. If such symptoms occur, discontinue AKYNZEO and initiate supportive treatment. If concomitant use of AKYNZEO with other serotonergic drugs is clinically warranted, patients should be made aware of a potential increased risk for serotonin syndrome.

Source: US FDA prescribing information

Side effects

The following clinically significant adverse reactions are found elsewhere in the labeling: Hypersensitivity Reactions Serotonin Syndrome Most common adverse reactions (≥3%) for AKYNZEO capsules are headache, asthenia, dyspepsia, fatigue, constipation and erythema. The safety profile of AKYNZEO for injection was generally similar to that seen with AKYNZEO capsules.

Source: US FDA prescribing information

Interactions

CYP3A4 Substrates: inhibition of CYP3A4 by netupitant can result in increased plasma concentrations of the concomitant drug for 6 days after single dosage administration of AKYNZEO, avoid concomitant CYP3A4 substrates for one week, if feasible. If not avoidable, consider dose reduction of the CYP3A4 substrate. CYP3A4 Inducers (e.g., rifampin): decreased plasma concentrations of netupitant, avoid use

Source: US FDA prescribing information

Storage

Storage AKYNZEO capsules should be stored at 20 °C to 25 °C (68 °F to 77 °F), excursions permitted from 15 °C to 30 °C (59 °F to 86 °F). NDC # 69639-102-01: pack of one vial of lyophilized powder Storage Store AKYNZEO for injection in carton, protected from light at 2° to 8°C (35.6 F to 46.4°F). NDC # 69639-106-01: pack of one vial of solution with hanger (Ready-to-Use) NDC # 69639-105-01: pack of one vial of solution (To-be-Diluted) Storage Store AKYNZEO injection in carton, protected from light at 20°C to 25°C (68°F to 77°F).

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 Netupitant and Palonosetron, sorted by availability.

MedicineActive ingredientManufacturerRegisterAvailability
Akynzeo 300 mg/0.5 mg capsuleOral Cold chainNetupitant and PalonosetronHelsinn TherapeuticsUS 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 10 October 2014Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Netupitant and Palonosetron available for export from India?

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

What brand names does Netupitant and Palonosetron have?

The catalogue lists 1 brand names for Netupitant and Palonosetron, including Akynzeo.

Is Netupitant and Palonosetron approved by the US FDA?

Yes. The US FDA first approved Netupitant and Palonosetron on 10 October 2014, according to Drugs@FDA.

Is Netupitant and Palonosetron authorised in the European Union?

Yes. Netupitant and Palonosetron has a central EU marketing authorisation (status: authorised), according to European Medicines Agency data.

Does Netupitant and Palonosetron need cold chain shipping?

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

Which ATC class is Netupitant and Palonosetron in?

Netupitant and Palonosetron is classified under ATC code A04AA (Anti-nausea and anti-vomiting medicines, subgroup A04A, subgroup A04AA).

References

  1. AKYNZEO prescribing information (Helsinn Therapeutics). U.S. National Library of Medicine, DailyMed. Retrieved 23 June 2026
  2. Akynzeo: European public assessment report (EPAR). European Medicines Agency. Retrieved 25 August 2026

Request Netupitant and Palonosetron for export supply

Tell us the strength, quantity and destination country. Our team replies with availability, lead time and the import documents needed.