60760-0658 Ondansetron Hydrochloride

Product NDC:

60760-0658

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: 60760-0658-10

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-10)

Effective Date: June 20, 2023

Discontinued:

Code: 60760-0658-15

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-15)

Effective Date: Sept. 15, 2025

Discontinued:

Code: 60760-0658-20

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-20)

Effective Date: June 23, 2025

Discontinued:

Code: 60760-0658-60

Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-658-60)

Effective Date: Oct. 30, 2025

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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