51655-0415 Ondansetron Hydrochloride

Product NDC:

51655-0415

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: 51655-0415-04

Description: 4 TABLET, FILM COATED in 1 BOTTLE (51655-415-04)

Effective Date: April 12, 2018

Discontinued:

Code: 51655-0415-43

Description: 3 TABLET, FILM COATED in 1 BOTTLE (51655-415-43)

Effective Date: Dec. 28, 2017

Discontinued:

Code: 51655-0415-53

Description: 10 TABLET, FILM COATED in 1 BOTTLE (51655-415-53)

Effective Date: April 24, 2018

Discontinued:

Code: 51655-0415-54

Description: 15 TABLET, FILM COATED in 1 BOTTLE (51655-415-54)

Effective Date: Dec. 28, 2017

Discontinued:

Code: 51655-0415-55

Description: 5 TABLET, FILM COATED in 1 BOTTLE (51655-415-55)

Effective Date: Dec. 7, 2017

Discontinued:

Code: 51655-0415-87

Description: 6 TABLET, FILM COATED in 1 BOTTLE (51655-415-87)

Effective Date: Oct. 24, 2018

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