00069-1340 Ondansetron Hydrochloride

Product NDC:

00069-1340

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

INJECTION, SOLUTION

Administration Route:

Intramuscular

Intravenous

Substances:

Name: Ondansetron Hydrochloride

Strength: 2.0

Unit: mg/mL

Packages:

Code: 00069-1340-02

Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0069-1340-02) > 20 mL in 1 VIAL, MULTI-DOSE

Effective Date: May 10, 2011

Discontinued: July 31, 2014

Code: 00069-1340-05

Description:

Effective Date: May 10, 2011

Discontinued: May 31, 2014

Code: 00069-1340-16

Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (0069-1340-16) > 2 mL in 1 VIAL, SINGLE-DOSE (0069-1340-05)

Effective Date: May 10, 2011

Discontinued: May 31, 2014

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

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