ONDANSETRON

Product NDC

70518-0021

11-digit product format

705180021

Labeler code

70518

Product ID

70518-0021_4303b1e1-ef93-5773-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ONDANSETRON

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077851

Marketing category

ANDA

Marketing start

2016-11-29

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record