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Ondansetron

Generic Name
Ondansetron
Brand Names
Zofran, Zuplenz
Drug Type
Small Molecule
Chemical Formula
C18H19N3O
CAS Number
99614-02-5
Unique Ingredient Identifier
4AF302ESOS

Overview

A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties. Having been developed in the 1980s by GlaxoSmithKline and approved by the US FDA since January 1991, ondansetron has demonstrated a long history of use and efficacy. Commonly formulated as oral tablets, orally disintegrating tablets (ODT), and injections, and available as generic products as well, ondansetron continues to see contemporary innovations in its formulation and use, including the development of orally soluble films that are both discreet in administration and less of a burden in comparison to having patients attempt to swallow pills during emesis. The FDA withdrew its approval for the use of all intravenous drug products containing more than 16 mg of ondansetron hydrochloride in a single dose, due to a high risk of QT prolongation.

Background

A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties. Having been developed in the 1980s by GlaxoSmithKline and approved by the US FDA since January 1991, ondansetron has demonstrated a long history of use and efficacy. Commonly formulated as oral tablets, orally disintegrating tablets (ODT), and injections, and available as generic products as well, ondansetron continues to see contemporary innovations in its formulation and use, including the development of orally soluble films that are both discreet in administration and less of a burden in comparison to having patients attempt to swallow pills during emesis. The FDA withdrew its approval for the use of all intravenous drug products containing more than 16 mg of ondansetron hydrochloride in a single dose, due to a high risk of QT prolongation.

Indication

In the adult patient population: i) orally administered ondansetron tablets and orally disintegrating tablets (ODT) are indicated for: - the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and radiotherapy, and - the prevention and treatment of postoperative nausea and vomiting ii) intravenously administered ondansetron injection formulations are indicated for: - the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, including high dose (ie. greater than or equal to 50 mg/m2) cisplatin therapy, and - the prevention and treatment of postoperative nausea and vomiting In the pediatric (4-18 years of age) patient population: i) ondansetron was effective and well tolerated when given to children 4-12 years of age for the treatment of post-chemotherapy induced nausea and vomiting, ii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for the treatment of children 3 years of age or younger, iii) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of post-radiotherapy induced nausea and vomiting, and iV) ondansetron tablets, ondansetron ODT, ondansetron injection are not indicated for use in any age group of the pediatric population for the treatment of postoperative nausea and vomiting In the geriatric (>65 years of age) patient population: i) efficacy and tolerance of ondansetron were similar to that observed in younger adults for the treatment of post-chemotherapy and radiotherapy-induced nausea and vomiting, and ii) clinical experience in the use of ondansetron in the prevention and treatment of postoperative nausea and vomiting is limited and is not indicated for use in the geriatric patient population

Associated Conditions

  • Chemotherapy-Induced Nausea and Vomiting
  • Cholestatic pruritus
  • Post Operative Nausea and Vomiting (PONV)
  • Radiation-Induced Nausea and Vomiting
  • Uremic Pruritus
  • Severe Hyperemesis gravidarum

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/04/16
Not Applicable
ENROLLING_BY_INVITATION
Nada kamel Elgamal
2025/03/27
Not Applicable
Completed
Muhammad Aamir Latif
2025/03/20
Phase 4
Completed
Hafiz Muhammad Hamza
2025/03/06
Phase 3
Recruiting
2025/02/27
Not Applicable
ENROLLING_BY_INVITATION
2025/02/06
Not Applicable
Recruiting
2024/12/10
Phase 2
Not yet recruiting
2024/11/25
Phase 4
Not yet recruiting
2024/11/20
Phase 4
Completed
The First Affiliated Hospital of Zhengzhou University
2024/06/26
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
DOH CENTRAL PHARMACY
53808-1121
ORAL
4 mg in 1 1
1/22/2019
American Health Packaging
68084-221
ORAL
8 mg in 1 1
8/1/2023
Dispensing Solutions, Inc.
55045-3817
ORAL
8 mg in 1 1
11/5/2013
Hikma Pharmaceuticals USA Inc.
0054-0064
ORAL
4 mg in 5 mL
10/4/2016
Aidarex Pharmaceuticals LLC
33261-747
ORAL
4 mg in 1 1
1/21/2014
Denton Pharma, Inc. dba Northwind Pharmaceuticals
70934-634
ORAL
4 mg in 1 1
1/1/2023
PD-Rx Pharmaceuticals, Inc.
43063-273
ORAL
8 mg in 1 1
9/26/2023
Proficient Rx LP
63187-483
ORAL
8 mg in 1 1
11/1/2018
Rebel Distributors Corp
42254-077
ORAL
4 mg in 1 1
11/16/2009
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
23155-549
INTRAVENOUS, INTRAMUSCULAR
2 mg in 1 mL
3/4/2022

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
ONDANSETRON-AFT SOLUTION FOR INJECTION 2MG/ML
SIN15006P
INJECTION, SOLUTION
2mg/ml
5/18/2016
ODNATRON Film Coated tablet 8 mg
SIN13714P
TABLET, FILM COATED
8mg
10/27/2009
NATZO 8 TABLETS 8 mg
SIN15424P
TABLET
8.0 mg
2/9/2018
Ondansetron Sandoz 8mg Tablets
SIN13446P
TABLET, FILM COATED
8mg
4/16/2008
ONDANSETRON FRESENIUS INJECTION 2MG/ML
SIN16020P
INJECTION, SOLUTION
2MG/ML
9/25/2020
ONDANSETRON B. BRAUN SOLUTION FOR INJECTION OR INFUSION 2 MG/ML
SIN15742P
INJECTION, SOLUTION
2.000mg/mL
7/10/2019
ONDAVELL FILM-COATED TABLET 8MG
SIN15004P
TABLET, FILM COATED
8mg
5/5/2016
NATZO 4 TABLETS 4mg
SIN15423P
TABLET
4 mg
2/9/2018
ONDA SOLUTION FOR INJECTION 2mg/ml
SIN15929P
INJECTION, SOLUTION
2.00mg/ml
4/13/2020
PREZINTON SOLUTION FOR INJECTION 4 MG/2ML
SIN16791P
INJECTION, SOLUTION
4mg/2ml
5/22/2023

NMPA Drug Approvals

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