35356-0652 Ondansetron Hydrochloride

Product NDC:

35356-0652

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: 35356-0652-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (35356-652-10)

Effective Date: April 3, 2012

Discontinued: June 1, 2016

Code: 35356-0652-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (35356-652-20)

Effective Date: April 3, 2012

Discontinued: June 1, 2016

Code: 35356-0652-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (35356-652-30)

Effective Date: April 3, 2012

Discontinued: June 1, 2016

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

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