00378-0315 Ondansetron

Product NDC:

00378-0315

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 4.0

Unit: mg/1

Packages:

Code: 00378-0315-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0315-01)

Effective Date: June 25, 2007

Discontinued:

Code: 00378-0315-05

Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0315-05)

Effective Date: June 25, 2007

Discontinued:

Code: 00378-0315-53

Description:

Effective Date: June 25, 2007

Discontinued: Aug. 7, 2011

Code: 00378-0315-93

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0315-93)

Effective Date: June 25, 2007

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