51079-0525 Ondansetron

Product NDC:

51079-0525

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 51079-0525-01

Description:

Effective Date: July 9, 2007

Discontinued: April 30, 2019

Code: 51079-0525-20

Description: 100 BLISTER PACK in 1 CARTON (51079-525-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-525-01)

Effective Date: July 9, 2007

Discontinued: April 30, 2019

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

CanMED and the Oncology Toolbox