Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

3 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	3 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
31631	34049	1034049	paketėlis	N7		Receptinis	EU/1/05/331/047	Netiekiama	-	-	No	-	-
31633	34051	1034051	paketėlis	N28		Receptinis	EU/1/05/331/049	Netiekiama	-	-	No	-	-
31634	34052	1034052	paketėlis	N30		Receptinis	EU/1/05/331/050	Netiekiama	-	-	No	-	-
31637	34055	1034055	paketėlis	N84		Receptinis	EU/1/05/331/053	Netiekiama	-	-	No	-	-
98164	84262	1084262	paketėlis	N14		Receptinis	EU/1/05/331/058	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas