51672-4108 Ondansetron Hydrochloride

Product NDC:

51672-4108

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: 51672-4108-00

Description: 1 BLISTER PACK in 1 CARTON (51672-4108-0) / 100 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: March 28, 2011

Discontinued:

Code: 51672-4108-06

Description: 30 TABLET, FILM COATED in 1 BOTTLE (51672-4108-6)

Effective Date: March 28, 2011

Discontinued:

Code: 51672-4108-08

Description: 1 BLISTER PACK in 1 CARTON (51672-4108-8) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: March 28, 2011

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