Granisetron

Product NDC

66758-036

11-digit product format

667580036

Labeler code

66758

Product ID

66758-036_81cd24a3-19ba-4ad8-ba90-da4f0a26f230

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Granisetron

Dosage form

INJECTION

Route

INTRAVENOUS

Labeler

Sandoz Inc.

Application

ANDA078835

Marketing category

ANDA

Marketing start

2008-06-30

Marketing end

2020-05-19

Substance

GRANISETRON HYDROCHLORIDE

Active strength

1 mg/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record