Neupro - 50474-801-03 - (rotigotine)

Alphabetical Index


Drug Information of Neupro

Product NDC: 50474-801
Proprietary Name: Neupro
Non Proprietary Name: rotigotine
Active Ingredient(s): 1    mg/24h & nbsp;   rotigotine
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Neupro

Product NDC: 50474-801
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021829
Marketing Category: NDA
Start Marketing Date: 20120402

Package Information of Neupro

Package NDC: 50474-801-03
Package Description: 30 POUCH in 1 CARTON (50474-801-03) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH

NDC Information of Neupro

NDC Code 50474-801-03
Proprietary Name Neupro
Package Description 30 POUCH in 1 CARTON (50474-801-03) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH
Product NDC 50474-801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rotigotine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20120402
Marketing Category Name NDA
Labeler Name UCB, Inc.
Substance Name ROTIGOTINE
Strength Number 1
Strength Unit mg/24h
Pharmaceutical Classes

Complete Information of Neupro


General Information