70934-0148 Ondansetron Hydrochloride

Product NDC:

70934-0148

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: 70934-0148-03

Description: 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-148-03)

Effective Date: Dec. 19, 2018

Discontinued: Nov. 30, 2023

Code: 70934-0148-04

Description: 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-148-04)

Effective Date: Aug. 6, 2018

Discontinued: Aug. 31, 2025

Code: 70934-0148-05

Description: 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-148-05)

Effective Date: July 29, 2019

Discontinued: Nov. 30, 2023

Code: 70934-0148-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-148-06)

Effective Date: Oct. 22, 2018

Discontinued: Nov. 30, 2023

Code: 70934-0148-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-148-10)

Effective Date: July 16, 2019

Discontinued: June 30, 2024

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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