xefo

Medicinal product

(Invented) name

xefo

Active substance (s)

Lornoksikamas

Strength

8 mg

Pharmaceutical form

milteliai ir tirpiklis injekciniam tirpalui

Route (s) of administration

leisti į veną, leisti į raumenis

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

M01AC05, Lornoxicam

Marketing authorisation holder

Takeda Austria GmbH, Austrija

Date of authorisation

1998-08-26

Date of renewal

2011-04-21

Documents

2432 Pakuotės lapelis milt inj 2023 07 10.docx

2432 xefo 8mg milt inj PCS PL 2023 07 10.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

DK/H/0123/005

Marketing authorisation procedure

Savitarpio pripažinimo procedūra

Qualitative and quantitative composition

Buteliuke yra	1 vnt.
Lornoksikamas	8 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
7668	12604	1012604	buteliukas	milteliai ir ampulė tirpiklio (2 ml) N1		Receptinis	LT/1/98/2432/015	Tiekiama	-	-	No	-	-
23784	4274	1004274	buteliukas	milteliai ir ampulė tirpiklio (2 ml) N5		Receptinis	LT/1/98/2432/016	Netiekiama	-	-	No	-	-	Download
23785	26469	1026469	buteliukas	milteliai ir ampulė tirpiklio (2 ml) N6		Receptinis	LT/1/98/2432/017	Netiekiama	-	-	No	-	-
23786	26470	1026470	buteliukas	milteliai ir ampulė tirpiklio (2 ml) N10		Receptinis	LT/1/98/2432/018	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2011-04-21	Perregistruotas
1998-08-26	Registruotas