Ondansetron

Product NDC

55154-5369

11-digit product format

551545369

Labeler code

55154

Product ID

55154-5369_919e5f97-9b6c-4326-bba3-afd3668bbc21

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ondansetron

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA076930

Marketing category

ANDA

Marketing start

2012-12-05

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

4 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record