ONDANSETRON

Product NDC

58118-0450

11-digit product format

581180450

Labeler code

58118

Product ID

58118-0450_5becd0eb-8a10-2245-e053-2a91aa0a9339

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ONDANSETRON

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Clinical Solutions Wholesale, LLC

Application

ANDA077851

Marketing category

ANDA

Marketing start

2007-06-25

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record