67046-0346 Ondansetron Hydrochloride

Product NDC:

67046-0346

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 4.0

Unit: mg/1

Packages:

Code: 67046-0346-03

Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-0346-3)

Effective Date: Nov. 8, 2024

Discontinued:

Code: 67046-0346-06

Description: 60 TABLET, FILM COATED in 1 BLISTER PACK (67046-0346-6)

Effective Date: Nov. 8, 2024

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

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