50090-1600 Ondansetron

Product NDC:

50090-1600

Brand Name:

Ondansetron

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: 50090-1600-00

Description: 10 TABLET, FILM COATED in 1 BOTTLE (50090-1600-0)

Effective Date: Jan. 5, 2015

Discontinued: May 31, 2019

Code: 50090-1600-01

Description: 6 TABLET, FILM COATED in 1 BOTTLE (50090-1600-1)

Effective Date: Jan. 5, 2015

Discontinued: Jan. 31, 2018

Code: 50090-1600-02

Description: 20 TABLET, FILM COATED in 1 BOTTLE (50090-1600-2)

Effective Date: Jan. 5, 2015

Discontinued: May 31, 2019

Code: 50090-1600-03

Description:

Effective Date: Jan. 5, 2015

Discontinued: Aug. 31, 2017

Code: 50090-1600-04

Description: 3 TABLET, FILM COATED in 1 BOTTLE (50090-1600-4)

Effective Date: Jan. 5, 2015

Discontinued: May 31, 2019

Code: 50090-1600-05

Description: 12 TABLET, FILM COATED in 1 BOTTLE (50090-1600-5)

Effective Date: Jan. 5, 2015

Discontinued: March 31, 2018

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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CanMED: NDC