63187-0636 Ondansetron Hydrochloride

Product NDC:

63187-0636

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: 63187-0636-01

Description: 1 TABLET, FILM COATED in 1 BOTTLE (63187-636-01)

Effective Date: Sept. 4, 2018

Discontinued:

Code: 63187-0636-03

Description: 3 TABLET, FILM COATED in 1 BOTTLE (63187-636-03)

Effective Date: May 1, 2017

Discontinued:

Code: 63187-0636-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (63187-636-06)

Effective Date: Aug. 1, 2019

Discontinued:

Code: 63187-0636-10

Description: 10 BLISTER PACK in 1 CARTON (63187-636-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: May 2, 2016

Discontinued:

Code: 63187-0636-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE (63187-636-12)

Effective Date: Sept. 4, 2018

Discontinued:

Code: 63187-0636-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE (63187-636-15)

Effective Date: May 2, 2016

Discontinued:

Code: 63187-0636-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (63187-636-20)

Effective Date: May 2, 2016

Discontinued:

Code: 63187-0636-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (63187-636-30)

Effective Date: May 2, 2016

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