Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

2 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	2 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
26981	29545	1029545	paketėlis	N7		Receptinis	EU/1/05/331/001	Netiekiama	-	-	No	-	-
26982	29546	1029546	paketėlis	N28		Receptinis	EU/1/05/331/002	Netiekiama	-	-	No	-	-
26985	29549	1029549	paketėlis	N30		Receptinis	EU/1/05/331/015	Netiekiama	-	-	No	-	-
26988	29552	1029552	paketėlis	N84		Receptinis	EU/1/05/331/018	Netiekiama	-	-	No	-	-
98162	84260	1084260	paketėlis	N14		Receptinis	EU/1/05/331/057	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas