63629-6709 Ondansetron Hydrochloride

Product NDC:

63629-6709

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Ondansetron Hydrochloride

Strength: 4.0

Unit: mg/1

Packages:

Code: 63629-6709-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (63629-6709-1)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 63629-6709-02

Description: 14 TABLET, FILM COATED in 1 BOTTLE (63629-6709-2)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 63629-6709-03

Description: 15 TABLET, FILM COATED in 1 BOTTLE (63629-6709-3)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 63629-6709-04

Description: 12 TABLET, FILM COATED in 1 BOTTLE (63629-6709-4)

Effective Date: Aug. 28, 2015

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