Ondansetron

Product NDC

70518-0480

11-digit product format

705180480

Labeler code

70518

Product ID

70518-0480_852b7414-7070-8492-e053-2991aa0a3bd3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ondansetron

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077851

Marketing category

ANDA

Marketing start

2017-05-03

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record