60760-0637 Ondansetron Hydrochloride

Product NDC:

60760-0637

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: 60760-0637-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-637-10)

Effective Date: July 31, 2007

Discontinued:

Code: 60760-0637-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-637-15)

Effective Date: June 3, 2020

Discontinued:

Code: 60760-0637-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-637-20)

Effective Date: March 13, 2018

Discontinued: Dec. 31, 2021

Code: 60760-0637-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-637-30)

Effective Date: Oct. 10, 2019

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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