58118-0458 Ondansetron

Product NDC:

58118-0458

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: 58118-0458-00

Description: 1 TABLET, FILM COATED in 1 PACKET (58118-0458-0)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-0458-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (58118-0458-3)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-0458-05

Description: 15 TABLET, FILM COATED in 1 BOTTLE (58118-0458-5)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-0458-06

Description: 60 TABLET, FILM COATED in 1 BOTTLE (58118-0458-6)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-0458-08

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0458-8)

Effective Date: June 25, 2007

Discontinued: June 26, 2017

Code: 58118-0458-09

Description: 90 TABLET, FILM COATED in 1 BOTTLE (58118-0458-9)

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