54569-6168 Ondansetron

Product NDC:

54569-6168

Brand Name:

Ondansetron

Generic Name:

Ondansetron

ondansetron hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 4.0

Unit: mg/1

Packages:

Code: 54569-6168-00

Description: 10 TABLET, FILM COATED in 1 BOTTLE (54569-6168-0)

Effective Date: May 9, 2016

Discontinued:

Code: 54569-6168-01

Description: 6 TABLET, FILM COATED in 1 BOTTLE (54569-6168-1)

Effective Date: May 9, 2016

Discontinued:

Code: 54569-6168-02

Description: 20 TABLET, FILM COATED in 1 BOTTLE (54569-6168-2)

Effective Date: May 9, 2016

Discontinued:

Code: 54569-6168-03

Description: 8 TABLET, FILM COATED in 1 BOTTLE (54569-6168-3)

Effective Date: May 9, 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