Granisetron Hydrochloride

Product NDC

0093-7485

11-digit product format

000937485

Labeler code

0093

Product ID

0093-7485_f1c6a9e1-14bb-4697-b2ee-e8e283adf6a8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Granisetron Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA078080

Marketing category

ANDA

Marketing start

2008-01-02

Marketing end

2019-09-30

Substance

GRANISETRON HYDROCHLORIDE

Active strength

1 mg/1

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