21695-0834 Ondansetron Hydrochloride

Product NDC:

21695-0834

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: 21695-0834-04

Description: 4 TABLET, FILM COATED in 1 BOTTLE (21695-834-04)

Effective Date: June 25, 2007

Discontinued:

Code: 21695-0834-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE (21695-834-12)

Effective Date: June 25, 2007

Discontinued:

Code: 21695-0834-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE (21695-834-15)

Effective Date: June 25, 2007

Discontinued:

Code: 21695-0834-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-834-30)

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