61786-0693 Ondansetron Hydrochloride

Product NDC:

61786-0693

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Ondansetron Hydrochloride

Strength: 4.0

Unit: mg/1

Packages:

Code: 61786-0693-02

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (61786-693-02)

Effective Date: May 19, 2016

Discontinued: Oct. 1, 2018

Code: 61786-0693-03

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-693-03)

Effective Date: April 21, 2017

Discontinued: Oct. 1, 2018

Code: 61786-0693-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-693-15)

Effective Date: July 11, 2017

Discontinued: Oct. 1, 2018

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

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