61919-0087 Ondansetron

Product NDC:

61919-0087

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 61919-0087-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (61919-087-10)

Effective Date: Aug. 29, 2019

Discontinued:

Code: 61919-0087-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE (61919-087-15)

Effective Date: Aug. 29, 2019

Discontinued:

Code: 61919-0087-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (61919-087-20)

Effective Date: March 10, 2017

Discontinued:

Code: 61919-0087-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (61919-087-30)

Effective Date: Aug. 29, 2019

Discontinued:

Code: 61919-0087-60

Description: 60 TABLET, FILM COATED in 1 BOTTLE (61919-087-60)

Effective Date: March 10, 2017

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