69339-0172 Ondansetron

Product NDC:

69339-0172

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 69339-0172-03

Description: 30 TABLET in 1 BOTTLE (69339-172-03)

Effective Date: Oct. 24, 2022

Discontinued:

Code: 69339-0172-01

Description: 100 TABLET in 1 BOTTLE (69339-172-01)

Effective Date: June 27, 2025

Discontinued:

Code: 69339-0172-05

Description: 500 TABLET in 1 BOTTLE (69339-172-05)

Effective Date: June 27, 2025

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox