70934-0318 Ondansetron Hydrochloride

Product NDC:

70934-0318

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: 70934-0318-03

Description: 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-318-03)

Effective Date: March 13, 2019

Discontinued: Oct. 31, 2024

Code: 70934-0318-04

Description: 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-318-04)

Effective Date: June 11, 2021

Discontinued: Oct. 31, 2024

Code: 70934-0318-05

Description: 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-318-05)

Effective Date: Sept. 27, 2021

Discontinued: Oct. 31, 2024

Code: 70934-0318-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-318-06)

Effective Date: Sept. 1, 2021

Discontinued: Oct. 31, 2024

Code: 70934-0318-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-318-10)

Effective Date: April 4, 2019

Discontinued: Feb. 28, 2025

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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