NEUPRO
NEUPRO
Approved
DIN Number
02403935
Drug Class
Human
Market Date
Jun 27, 2013
Company
HC
UCB Canada Inc
Product Information
Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.
Product Details
Health Canada regulatory and product classification information
Regulatory Identifiers
DIN Number02403935
AIG Number0154150005
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
N04BC09 ROTIGOTINE
Product Specifications
Dosage FormPatch
Route of AdministrationTransdermal
AHFS Classification28:36.20.08
Health Canada Classification
ACTIVE INGREDIENTS (1)
ROTIGOTINEActive
Strength: 6 MG / 24 HOUR
Monograph: ROTIGOTINE