83980-0017 Ondansetron hydrochloride

Product NDC:

83980-0017

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: 83980-0017-10

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (83980-017-10)

Effective Date: Aug. 14, 2026

Discontinued:

Code: 83980-0017-13

Description: 30 TABLET, FILM COATED in 1 BOTTLE (83980-017-13)

Effective Date: Aug. 14, 2026

Discontinued:

Code: 83980-0017-97

Description: 10 TABLET, FILM COATED in 1 BOTTLE (83980-017-97)

Effective Date: Aug. 14, 2026

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