Sancuso - 54868-5985-0 - (granisetron)

Alphabetical Index


Drug Information of Sancuso

Product NDC: 54868-5985
Proprietary Name: Sancuso
Non Proprietary Name: granisetron
Active Ingredient(s): 3.1    mg/24h & nbsp;   granisetron
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Sancuso

Product NDC: 54868-5985
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022198
Marketing Category: NDA
Start Marketing Date: 20090216

Package Information of Sancuso

Package NDC: 54868-5985-0
Package Description: 1 POUCH in 1 CARTON (54868-5985-0) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH

NDC Information of Sancuso

NDC Code 54868-5985-0
Proprietary Name Sancuso
Package Description 1 POUCH in 1 CARTON (54868-5985-0) > 1 PATCH in 1 POUCH > 168 h in 1 PATCH
Product NDC 54868-5985
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name granisetron
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20090216
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name GRANISETRON
Strength Number 3.1
Strength Unit mg/24h
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Sancuso


General Information