67296-0902 Ondansetron Hydrochloride

Product NDC:

67296-0902

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: 67296-0902-01

Description: 3 TABLET, FILM COATED in 1 BOTTLE (67296-0902-1)

Effective Date: July 31, 2007

Discontinued:

Code: 67296-0902-02

Description: 20 TABLET, FILM COATED in 1 BOTTLE (67296-0902-2)

Effective Date: Jan. 1, 2021

Discontinued:

Code: 67296-0902-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (67296-0902-3)

Effective Date: July 31, 2007

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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