Elontril

Medicinal product

(Invented) name

Elontril

Active substance (s)

Bupropiono hidrochloridas

Strength

150 mg

Pharmaceutical form

modifikuoto atpalaidavimo tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

N06AX12, Bupropion

Marketing authorisation holder

GlaxoSmithKline Trading Services Limited, Airija

Date of authorisation

2007-04-12

Date of renewal

2012-01-27

Documents

0705 Pakuotės lapelis 2025 03 03.docx

0705 Elontril II PL 2025 03 03.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

NL/H/0786/001/DC

Marketing authorisation procedure

Decentralizuota procedūra

Qualitative and quantitative composition

Tabletėje yra	1 vnt.
Bupropiono hidrochloridas	150 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
18940	22436	1022436	buteliukas	N7		Receptinis	LT/1/07/0705/001	Netiekiama	-	-	No	-	-
22249	4747	1004747	buteliukas	N30		Receptinis	LT/1/07/0705/002	Tiekiama	2025-08-28	-	No	-	-	Download
22250	25048	1025048	buteliukas	N90 (3x30)		Receptinis	LT/1/07/0705/003	Netiekiama	-	-	No	-	-
108991	95097	1095097	buteliukas	N90		Receptinis	LT/1/07/0705/007	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2012-01-27	Perregistruotas
2007-04-12	Registruotas