HELIXOR P

Medicinal product

(Invented) name

HELIXOR P

Active substance (s)

Pušų amalų (Viscum album ssp. pini) skystasis ekstraktas (1:20)

Strength

20 mg/ml

Pharmaceutical form

injekcinis tirpalas

Route (s) of administration

leisti po oda

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

Nesuteiktas, Netaikoma ar nesuteiktas

Marketing authorisation holder

Helixor Heilmittel GmbH , Vokietija

Date of authorisation

2004-03-09

Date of renewal

2014-04-22

Documents

0056_0057_0058 Pakuotės lapelis 2016 02 02.docx

0056_0057_0058 Helixor A_M_P inj RPP 2016 02 02t.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

10a

Procedure number

Marketing authorisation procedure

Nacionalinė procedūra

Qualitative and quantitative composition

Ampulėje (1 ml tirpalo) yra	1 ml
Pušų amalų (Viscum album ssp. pini) skystasis ekstraktas (1:20)	20 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
7974	12800	1012800	ampulė	1 ml N8		Receptinis	LT/1/04/0058/009	Netiekiama	-	-	No	-	-
7975	12801	1012801	ampulė	1 ml N50		Receptinis	LT/1/04/0058/010	Netiekiama	-	-	No	-	-
61684	76025	1076025	ampulė	1 ml N6		Receptinis	LT/1/04/0058/023	Tiekiama	-	-	No	-	-	Download

Stadijos

Data	Stadija
2014-04-22	Perregistruotas
2004-03-09	Registruotas