70934-0193 Ondansetron Hydrochloride

Product NDC:

70934-0193

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: 70934-0193-06

Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-193-06)

Effective Date: Feb. 28, 2019

Discontinued: Dec. 31, 2023

Code: 70934-0193-12

Description: 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-193-12)

Effective Date: Nov. 12, 2018

Discontinued: Dec. 31, 2023

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

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