68788-9402 Ondansetron Hydrochloride

Product NDC:

68788-9402

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: 68788-9402-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-9402-1)

Effective Date: June 12, 2012

Discontinued:

Code: 68788-9402-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9402-3)

Effective Date: June 12, 2012

Discontinued:

Code: 68788-9402-05

Description: 15 TABLET, FILM COATED in 1 BOTTLE (68788-9402-5)

Effective Date: June 23, 2017

Discontinued:

Code: 68788-9402-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (68788-9402-6)

Effective Date: June 23, 2017

Discontinued:

Code: 68788-9402-02

Description: 12 TABLET, FILM COATED in 1 BOTTLE (68788-9402-2)

Effective Date: June 23, 2017

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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