54868-5738 Ondansetron Hydrochloride

Product NDC:

54868-5738

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: 54868-5738-00

Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5738-0)

Effective Date: Dec. 29, 2006

Discontinued:

Code: 54868-5738-01

Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5738-1)

Effective Date: Dec. 29, 2006

Discontinued:

Code: 54868-5738-02

Description: 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5738-2)

Effective Date: Dec. 29, 2006

Discontinued:

Code: 54868-5738-03

Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-5738-3)

Effective Date: Dec. 29, 2006

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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