50436-0132 Ondansetron

Product NDC:

50436-0132

Brand Name:

Ondansetron

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: 50436-0132-01

Description: 30 TABLET, FILM COATED in 1 BOTTLE (50436-0132-1)

Effective Date: June 25, 2007

Discontinued:

Code: 50436-0132-04

Description: 10 TABLET, FILM COATED in 1 BOTTLE (50436-0132-4)

Effective Date: June 25, 2007

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