55700-0631 Ondansetron Hydrochloride

Product NDC:

55700-0631

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: 55700-0631-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (55700-631-06)

Effective Date: May 25, 2018

Discontinued:

Code: 55700-0631-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (55700-631-10)

Effective Date: May 25, 2018

Discontinued:

Code: 55700-0631-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (55700-631-20)

Effective Date: May 25, 2018

Discontinued:

Code: 55700-0631-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (55700-631-30)

Effective Date: May 25, 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