63187-0709 Ondansetron Hydrochloride

Product NDC:

63187-0709

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: 63187-0709-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (63187-709-06)

Effective Date: March 1, 2019

Discontinued:

Code: 63187-0709-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (63187-709-10)

Effective Date: June 1, 2016

Discontinued:

Code: 63187-0709-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE (63187-709-15)

Effective Date: June 1, 2016

Discontinued:

Code: 63187-0709-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (63187-709-20)

Effective Date: June 1, 2016

Discontinued:

Code: 63187-0709-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (63187-709-30)

Effective Date: June 1, 2016

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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