58118-1459 Ondansetron

Product NDC:

58118-1459

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: 58118-1459-00

Description: 1 TABLET, FILM COATED in 1 PACKET (58118-1459-0)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-1459-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (58118-1459-3)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-1459-05

Description: 15 TABLET, FILM COATED in 1 BOTTLE (58118-1459-5)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-1459-06

Description: 60 TABLET, FILM COATED in 1 BOTTLE (58118-1459-6)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-1459-08

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-1459-8)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-1459-09

Description: 90 TABLET, FILM COATED in 1 BOTTLE (58118-1459-9)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

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

CanMED: NDC