33261-0417 Ondansetron Hydrochloride

Product NDC:

33261-0417

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: 33261-0417-05

Description: 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-05)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-06)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-09

Description: 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-09)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-10)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-12)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-15)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-20)

Effective Date: July 31, 2007

Discontinued:

Code: 33261-0417-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-417-30)

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