Ondansetron

Product NDC

68071-1547

11-digit product format

680711547

Labeler code

68071

Product ID

68071-1547_553fcc9e-b728-07ac-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ondansetron

Dosage form

TABLET, ORALLY DISINTEGRATING

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA078152

Marketing category

ANDA

Marketing start

2007-06-27

Marketing end

0000-00-00

Substance

ONDANSETRON

Active strength

8 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