ondansetron

Product NDC

71335-0831

11-digit product format

713350831

Labeler code

71335

Product ID

71335-0831_1b2bcd7d-edb8-4dc3-9933-36e6c8777000

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ondansetron

Dosage form

TABLET, ORALLY DISINTEGRATING

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077557

Marketing category

ANDA

Marketing start

2007-08-02

Marketing end

0000-00-00

Substance

ONDANSETRON

Active strength

4 mg/1

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