60760-0636 Ondansetron Hydrochloride

Product NDC:

60760-0636

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: 60760-0636-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10)

Effective Date: July 31, 2007

Discontinued:

Code: 60760-0636-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20)

Effective Date: March 26, 2018

Discontinued:

Code: 60760-0636-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-30)

Effective Date: Oct. 15, 2019

Discontinued:

Code: 60760-0636-16

Description: 16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16)

Effective Date: March 3, 2023

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