35356-0853 Ondansetron

Product NDC:

35356-0853

Brand Name:

Ondansetron

Generic Name:

Ondansetron

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 4.0

Unit: mg/1

Packages:

Code: 35356-0853-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE (35356-853-06)

Effective Date: Dec. 11, 2015

Discontinued:

Code: 35356-0853-09

Description: 9 TABLET, FILM COATED in 1 BOTTLE (35356-853-09)

Effective Date: Dec. 11, 2015

Discontinued:

Code: 35356-0853-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE (35356-853-10)

Effective Date: July 27, 2007

Discontinued:

Code: 35356-0853-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE (35356-853-20)

Effective Date: July 27, 2007

Discontinued:

Code: 35356-0853-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (35356-853-30)

Effective Date: July 27, 2007

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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