Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

8 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	8 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
27008	29572	1029572	paketėlis	N7		Receptinis	EU/1/05/331/010	Netiekiama	-	-	No	-	-
27009	29573	1029573	paketėlis	N28		Receptinis	EU/1/05/331/011	Netiekiama	-	-	No	-	-
27012	29576	1029576	paketėlis	N30		Receptinis	EU/1/05/331/033	Netiekiama	-	-	No	-	-
27015	29579	1029579	paketėlis	N84		Receptinis	EU/1/05/331/036	Netiekiama	-	-	No	-	-
98161	84259	1084259	paketėlis	N14		Receptinis	EU/1/05/331/061	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas