54348-0821 Ondansetron Hydrochloride

Product NDC:

54348-0821

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: 54348-0821-00

Description: 1 BOTTLE in 1 BOX (54348-821-00) / 1 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 8, 2019

Discontinued:

Code: 54348-0821-02

Description: 1 BOTTLE in 1 BOX (54348-821-02) / 2 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 8, 2019

Discontinued:

Code: 54348-0821-04

Description: 1 BOTTLE in 1 BOX (54348-821-04) / 4 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 8, 2019

Discontinued:

Code: 54348-0821-05

Description: 1 BOTTLE in 1 BOX (54348-821-05) / 5 TABLET, FILM COATED in 1 BOTTLE

Effective Date: Aug. 8, 2019

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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