Ondansetron Hydrochloride

Product NDC

55154-4731

11-digit product format

551544731

Labeler code

55154

Product ID

55154-4731_db4f834b-9882-438e-9c0b-210bba6b398e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ONDANSETRON HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Cardinal Health

Application

ANDA077548

Marketing category

ANDA

Marketing start

2006-12-26

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

2 mg/mL

Pharmacologic classes

Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record