Ondansetron Hydrochloride

Product NDC

23155-378

11-digit product format

231550378

Labeler code

23155

Product ID

23155-378_4f9386bf-c714-47a0-b2f9-228dc0acb0a2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ondansetron Hydrochloride

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Heritage Pharmaceuticals Inc.

Application

ANDA078945

Marketing category

ANDA

Marketing start

2014-02-19

Marketing end

0000-00-00

Substance

ONDANSETRON HYDROCHLORIDE

Active strength

2 mg/mL

Pharmacologic classes

Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record