68788-8651 Ondansetron Hydrochloride - CanMED: NDC

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Product Information

CanMED: NDC

Product NDC:

68788-8651

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: 68788-8651-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-8651-1)

Effective Date: April 29, 2024

Discontinued:

Code: 68788-8651-02

Description: 12 TABLET, FILM COATED in 1 BOTTLE (68788-8651-2)

Effective Date: April 29, 2024

Discontinued:

Code: 68788-8651-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-8651-3)

Effective Date: April 29, 2024

Discontinued:

Code: 68788-8651-05

Description: 15 TABLET, FILM COATED in 1 BOTTLE (68788-8651-5)

Effective Date: April 29, 2024

Discontinued:

Code: 68788-8651-06

Description: 60 TABLET, FILM COATED in 1 BOTTLE (68788-8651-6)

Effective Date: April 29, 2024

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use