Home > National Drug Code (NDC) > Granisetron Hydrochloride

Granisetron Hydrochloride - 16714-221-01 - (Granisetron Hydrochloride)

Alphabetical Index


Drug Information of Granisetron Hydrochloride

Product NDC: 16714-221
Proprietary Name: Granisetron Hydrochloride
Non Proprietary Name: Granisetron Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Granisetron Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Granisetron Hydrochloride

Product NDC: 16714-221
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078678
Marketing Category: ANDA
Start Marketing Date: 20080429

Package Information of Granisetron Hydrochloride

Package NDC: 16714-221-01
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (16714-221-01)

NDC Information of Granisetron Hydrochloride

NDC Code 16714-221-01
Proprietary Name Granisetron Hydrochloride
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (16714-221-01)
Product NDC 16714-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080429
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name GRANISETRON HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Granisetron Hydrochloride


General Information