54348-0819 Ondansetron

Product NDC:

54348-0819

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: 54348-0819-00

Description: 1 BOTTLE in 1 BOX (54348-819-00) / 1 TABLET, FILM COATED in 1 BOTTLE

Effective Date: July 10, 2019

Discontinued:

Code: 54348-0819-02

Description: 1 BOTTLE in 1 BOX (54348-819-02) / 2 TABLET, FILM COATED in 1 BOTTLE

Effective Date: July 10, 2019

Discontinued:

Code: 54348-0819-04

Description: 1 BOTTLE in 1 BOX (54348-819-04) / 4 TABLET, FILM COATED in 1 BOTTLE

Effective Date: July 10, 2019

Discontinued:

Code: 54348-0819-06

Description: 1 BOTTLE in 1 BOX (54348-819-06) / 6 TABLET, FILM COATED in 1 BOTTLE

Effective Date: July 10, 2019

Discontinued:

Code: 54348-0819-08

Description: 1 BOTTLE in 1 BOX (54348-819-08) / 8 TABLET, FILM COATED in 1 BOTTLE

Effective Date: July 10, 2019

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