63629-5083 Ondansetron

Product NDC:

63629-5083

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 4.0

Unit: mg/1

Packages:

Code: 63629-5083-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (63629-5083-1)

Effective Date: Aug. 29, 2013

Discontinued:

Code: 63629-5083-02

Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-5083-2)

Effective Date: Feb. 8, 2022

Discontinued:

Code: 63629-5083-03

Description: 60 TABLET, FILM COATED in 1 BOTTLE (63629-5083-3)

Effective Date: Feb. 11, 2016

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