Ondansetron

Product NDC

0143-2423

11-digit product format

001432423

Labeler code

0143

Product ID

0143-2423_ebd1e2c0-535e-4fd7-b679-177e91e68687

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ondansetron hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA077545

Marketing category

ANDA

Marketing start

2008-01-01

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

8 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record