alli

Medicinal product

(Invented) name

alli

Active substance (s)

Orlistatas

Strength

27 mg

Pharmaceutical form

kramtomosios tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Nereceptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

A08AB01, Orlistat

Marketing authorisation holder

GlaxoSmithKline Dungarvan Limited, Airija

Date of authorisation

2007-07-23

Date of renewal

Documents

Search in EMA Europe

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

10c

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Chewable tablet	1 vnt.
Orlistatas	27 mg

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
44107	57897	1057897	buteliukas	N42		Nereceptinis	EU/1/07/401/012	Netiekiama	-	-	No	-	-
44108	57898	1057898	buteliukas	N60		Nereceptinis	EU/1/07/401/013	Netiekiama	-	-	No	-	-
44109	57899	1057899	buteliukas	N84		Nereceptinis	EU/1/07/401/014	Netiekiama	-	-	No	-	-
44110	57900	1057900	buteliukas	N90		Nereceptinis	EU/1/07/401/015	Netiekiama	-	-	No	-	-
49761	63632	1063632	buteliukas	N120		Nereceptinis	EU/1/07/401/016	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2020-07-22	Išregistruotas
2007-07-23	Registruotas