51655-0016 Ondansetron Hydrochloride

Product NDC:

51655-0016

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: 51655-0016-27

Description: 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-27)

Effective Date: Sept. 16, 2022

Discontinued:

Code: 51655-0016-53

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-53)

Effective Date: Sept. 16, 2022

Discontinued:

Code: 51655-0016-54

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-54)

Effective Date: Aug. 8, 2022

Discontinued:

Code: 51655-0016-87

Description: 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-016-87)

Effective Date: Sept. 21, 2022

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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