Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

4 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	4 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
26990	29554	1029554	paketėlis	N7		Receptinis	EU/1/05/331/004	Netiekiama	-	-	No	-	-
26991	29555	1029555	paketėlis	N28		Receptinis	EU/1/05/331/005	Netiekiama	-	-	No	-	-
26994	29558	1029558	paketėlis	N30		Receptinis	EU/1/05/331/021	Netiekiama	-	-	No	-	-
26997	29561	1029561	paketėlis	N84		Receptinis	EU/1/05/331/024	Netiekiama	-	-	No	-	-
98160	84258	1084258	paketėlis	N14		Receptinis	EU/1/05/331/059	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas