ondansetron

Product NDC

0179-0099

11-digit product format

001790099

Labeler code

0179

Product ID

0179-0099_7bebe842-759a-c53c-e053-2a91aa0ac993

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ondansetron hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA077851

Marketing category

ANDA

Marketing start

2011-09-12

Marketing end

2020-01-31

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

0000-00-00

Current FDA listing

Historical FDA.report record