68788-8582 Ondansetron Hydrochloride

Product NDC:

68788-8582

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 68788-8582-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-8582-1)

Effective Date: Feb. 12, 2024

Discontinued:

Code: 68788-8582-02

Description: 12 TABLET, FILM COATED in 1 BOTTLE (68788-8582-2)

Effective Date: Feb. 12, 2024

Discontinued:

Code: 68788-8582-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-8582-3)

Effective Date: Feb. 12, 2024

Discontinued:

Code: 68788-8582-05

Description: 15 TABLET, FILM COATED in 1 BOTTLE (68788-8582-5)

Effective Date: Feb. 12, 2024

Discontinued:

Code: 68788-8582-06

Description: 60 TABLET, FILM COATED in 1 BOTTLE (68788-8582-6)

Effective Date: Feb. 12, 2024

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED: NDC