65862-0187 Ondansetron Hydrochloride

Product NDC:

65862-0187

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: 65862-0187-03

Description: 1 BLISTER PACK in 1 CARTON (65862-187-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: July 31, 2007

Discontinued:

Code: 65862-0187-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE (65862-187-05)

Effective Date: July 31, 2007

Discontinued:

Code: 65862-0187-10

Description: 10 BLISTER PACK in 1 CARTON (65862-187-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: July 31, 2007

Discontinued:

Code: 65862-0187-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-187-30)

Effective Date: July 31, 2007

Discontinued:

Code: 65862-0187-81

Description:

Effective Date: July 31, 2007

Discontinued: Nov. 7, 2011

Code: 65862-0187-99

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-187-99)

Effective Date: July 31, 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

CanMED: NDC