70518-1042 Ondansetron hydrochloride

Product NDC:

70518-1042

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: 70518-1042-00

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1042-0)

Effective Date: March 1, 2018

Discontinued: May 11, 2020

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox