61919-0465 Ondansetron Hydrochloride

Product NDC:

61919-0465

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: 61919-0465-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (61919-465-06)

Effective Date: Jan. 1, 2014

Discontinued:

Code: 61919-0465-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (61919-465-10)

Effective Date: Jan. 1, 2014

Discontinued:

Code: 61919-0465-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (61919-465-30)

Effective Date: Jan. 1, 2014

Discontinued:

Code: 61919-0465-60

Description: 60 TABLET, FILM COATED in 1 BOTTLE (61919-465-60)

Effective Date: Jan. 1, 2014

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED: NDC