Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

1 mg/24 val.

Pharmaceutical form

transderminis pleistras

Route (s) of administration

vartoti per odą

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

N04BC09, Rotigotine

Marketing authorisation holder

UCB Pharma S.A., Belgija

Date of authorisation

2006-02-15

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Transdermal patch	1 vnt.
Rotigotinas	1 mg/24 val.

Packages

PAKID	NPAKID	NPAKID-7	Pack type	Pack size	Type of packaging	Proposed dispensing/classification	Marketing authorisation no.	Supply status	From	To	Package is in foreign language	From	To	Mock-up
31622	34040	1034040	paketėlis	N7		Receptinis	EU/1/05/331/038	Netiekiama	-	-	No	-	-
31624	34042	1034042	paketėlis	N28		Receptinis	EU/1/05/331/040	Netiekiama	-	-	No	-	-
31625	34043	1034043	paketėlis	N30		Receptinis	EU/1/05/331/041	Netiekiama	-	-	No	-	-
31628	34046	1034046	paketėlis	N84		Receptinis	EU/1/05/331/044	Netiekiama	-	-	No	-	-
98159	84257	1084257	paketėlis	N14		Receptinis	EU/1/05/331/056	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas