68788-9368 Ondansetron Hydrochloride

Product NDC:

68788-9368

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: 68788-9368-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-9368-1)

Effective Date: June 12, 2012

Discontinued:

Code: 68788-9368-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9368-3)

Effective Date: June 12, 2012

Discontinued:

Code: 68788-9368-08

Description:

Effective Date: Aug. 27, 2014

Discontinued: April 28, 2015

Code: 68788-9368-02

Description: 12 TABLET, FILM COATED in 1 BOTTLE (68788-9368-2)

Effective Date: June 23, 2017

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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