70518-4145 Ondansetron Hydrochloride

Product NDC:

70518-4145

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: 70518-4145-00

Description: 16 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-0)

Effective Date: July 18, 2024

Discontinued:

Code: 70518-4145-02

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-2)

Effective Date: Dec. 20, 2024

Discontinued:

Code: 70518-4145-01

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4145-1)

Effective Date: July 18, 2024

Discontinued:

Code: 70518-4145-03

Description: 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4145-3)

Effective Date: April 2, 2025

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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