50090-1015 Ondansetron

Product NDC:

50090-1015

Brand Name:

Ondansetron

Generic Name:

ondansetron hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 50090-1015-00

Description: 4 TABLET, FILM COATED in 1 BOTTLE (50090-1015-0)

Effective Date: Nov. 28, 2014

Discontinued: March 31, 2019

Code: 50090-1015-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (50090-1015-1)

Effective Date: Nov. 28, 2014

Discontinued: March 31, 2019

Code: 50090-1015-02

Description: 3 TABLET, FILM COATED in 1 BOTTLE (50090-1015-2)

Effective Date: Nov. 28, 2014

Discontinued: March 31, 2019

Code: 50090-1015-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (50090-1015-3)

Effective Date: Nov. 28, 2014

Discontinued: March 31, 2019

Code: 50090-1015-04

Description: 6 TABLET, FILM COATED in 1 BOTTLE (50090-1015-4)

Effective Date: Nov. 28, 2014

Discontinued: March 31, 2019

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox