54868-5801 Ondansetron Hydrochloride

Product NDC:

54868-5801

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: 54868-5801-00

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5801-0)

Effective Date: July 30, 2007

Discontinued:

Code: 54868-5801-01

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5801-1)

Effective Date: July 30, 2007

Discontinued:

Code: 54868-5801-02

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5801-2)

Effective Date: July 30, 2007

Discontinued:

Code: 54868-5801-03

Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5801-3)

Effective Date: July 30, 2007

Discontinued:

Code: 54868-5801-04

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5801-4)

Effective Date: July 30, 2007

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED: NDC