61919-0565 Ondansetron

Product NDC:

61919-0565

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: 61919-0565-10

Description: 1 TABLET, FILM COATED in 1 BOTTLE (61919-565-10)

Effective Date: Sept. 12, 2018

Discontinued:

Code: 61919-0565-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE (61919-565-12)

Effective Date: Sept. 6, 2019

Discontinued:

Code: 61919-0565-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (61919-565-20)

Effective Date: March 23, 2016

Discontinued:

Code: 61919-0565-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)

Effective Date: Aug. 22, 2019

Discontinued:

Code: 61919-0565-90

Description: 90 TABLET, FILM COATED in 1 BOTTLE (61919-565-90)

Effective Date: Aug. 22, 2019

Discontinued:

Code: 61919-0565-60

Description: 60 TABLET, FILM COATED in 1 BOTTLE (61919-565-60)

Effective Date: Sept. 6, 2019

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

Government Funding Lapse

CanMED: NDC

CanMED and the Oncology Toolbox

CanMED: NDC