00781-1679 Ondansetron

Product NDC:

00781-1679

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: 00781-1679-01

Description:

Effective Date: June 25, 2007

Discontinued: Dec. 1, 2015

Code: 00781-1679-13

Description:

Effective Date: June 25, 2007

Discontinued: Dec. 1, 2015

Code: 00781-1679-31

Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-1679-31)

Effective Date: June 25, 2007

Discontinued: July 31, 2019

Code: 00781-1679-33

Description: 1 BLISTER PACK in 1 CARTON (0781-1679-33) > 3 TABLET, FILM COATED in 1 BLISTER PACK

Effective Date: June 25, 2007

Discontinued: July 31, 2019

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

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