65862-0189 Ondansetron Hydrochloride

Product NDC:

65862-0189

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Ondansetron Hydrochloride

Strength: 24.0

Unit: mg/1

Packages:

Code: 65862-0189-11

Description: 1 BLISTER PACK in 1 CARTON (65862-189-11) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: July 31, 2007

Discontinued:

Code: 65862-0189-22

Description:

Effective Date: July 31, 2007

Discontinued: Nov. 7, 2011

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox