00703-7221 Ondansetron

Product NDC:

00703-7221

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

INJECTION, SOLUTION

Administration Route:

Intramuscular

Intravenous

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 2.0

Unit: mg/mL

Packages:

Code: 00703-7221-01

Description:

Effective Date: Nov. 22, 2006

Discontinued: May 31, 2018

Code: 00703-7221-02

Description:

Effective Date: Nov. 22, 2006

Discontinued: Dec. 27, 2011

Code: 00703-7221-03

Description:

Effective Date: Nov. 22, 2006

Discontinued: Dec. 27, 2011

Code: 00703-7221-04

Description: 25 VIAL, SINGLE-USE in 1 CARTON (0703-7221-04) > 2 mL in 1 VIAL, SINGLE-USE (0703-7221-01)

Effective Date: Nov. 22, 2006

Discontinued: May 31, 2018

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

CanMED: NDC