Neupro

Medicinal product

(Invented) name

Neupro

Active substance (s)

Rotigotinas

Strength

6 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	6 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
26999	29563	1029563	paketėlis	N7		Receptinis	EU/1/05/331/007	Netiekiama	-	-	No	-	-
27000	29564	1029564	paketėlis	N28		Receptinis	EU/1/05/331/008	Netiekiama	-	-	No	-	-
27003	29567	1029567	paketėlis	N30		Receptinis	EU/1/05/331/027	Netiekiama	-	-	No	-	-
27006	29570	1029570	paketėlis	N84		Receptinis	EU/1/05/331/030	Netiekiama	-	-	No	-	-
98163	84261	1084261	paketėlis	N14		Receptinis	EU/1/05/331/060	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2006-02-15	Registruotas