Ondansetron

Product NDC

65293-374

11-digit product format

652930374

Labeler code

65293

Product ID

65293-374_99d569d6-8690-560b-e053-2a95a90a0780

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ONDANSETRON HYDROCHLORIDE

Dosage form

INJECTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

The Medicines Company

Application

ANDA076974

Marketing category

ANDA

Marketing start

2009-11-18

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

2020-12-31

Current FDA listing

Historical FDA.report record