67296-1562 Ondansetron Hydrochloride

Product NDC:

67296-1562

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: 67296-1562-03

Description: 3 TABLET, FILM COATED in 1 BOTTLE (67296-1562-3)

Effective Date: Jan. 1, 2018

Discontinued:

Code: 67296-1562-02

Description: 20 TABLET, FILM COATED in 1 BOTTLE (67296-1562-2)

Effective Date: Jan. 1, 2018

Discontinued:

Code: 67296-1562-01

Description: 30 TABLET, FILM COATED in 1 BOTTLE (67296-1562-1)

Effective Date: Jan. 1, 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