Granisetron Hydrochloride

Product NDC

51672-4138

11-digit product format

516724138

Labeler code

51672

Product ID

51672-4138_792dd502-e445-4b74-b5f9-a946e4c3f57e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Granisetron Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Taro Pharmaceuticals U.S.A., Inc.

Application

ANDA090817

Marketing category

ANDA

Marketing start

2010-05-28

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record