55700-0064 Ondansetron

Product NDC:

55700-0064

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 55700-0064-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (55700-064-06)

Effective Date: Nov. 20, 2015

Discontinued: June 30, 2019

Code: 55700-0064-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (55700-064-10)

Effective Date: Nov. 20, 2015

Discontinued: June 30, 2019

Code: 55700-0064-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE (55700-064-12)

Effective Date: Nov. 20, 2015

Discontinued: June 30, 2019

Code: 55700-0064-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (55700-064-20)

Effective Date: Nov. 20, 2015

Discontinued: June 30, 2019

Code: 55700-0064-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (55700-064-30)

Effective Date: Nov. 20, 2015

Discontinued: June 30, 2019

Code: 55700-0064-60

Description:

Effective Date: Nov. 20, 2015

Discontinued: Jan. 12, 2016

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox

CanMED: NDC