ONDANSETRON

Product NDC

50090-2342

11-digit product format

500902342

Labeler code

50090

Product ID

50090-2342_e69ed61e-ffe3-4cf6-ac2c-a66c2d20b85c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ONDANSETRON

Dosage form

INJECTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

A-S Medication Solutions

Application

ANDA079224

Marketing category

ANDA

Marketing start

2012-06-15

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record