Diafer

Medicinal product

(Invented) name

Diafer

Active substance (s)

Geležis

Strength

50 mg/ml

Pharmaceutical form

injekcinis tirpalas

Route (s) of administration

leisti į veną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

B03AC, Iron, parenteral preparations

Marketing authorisation holder

Pharmacosmos A/S, Danija

Date of authorisation

2014-03-24

Date of renewal

Documents

3523_1_4 Diafer inj tirp RPP keit.docx

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

SE/H/1164/001/E/001

Marketing authorisation procedure

Kartotinė procedūra

Qualitative and quantitative composition

Viename mililitre tirpalo yra	1 ml
Geležis	50 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
57071	71183	1071183	ampulė	2 ml N1		Receptinis	LT/1/14/3523/001	Netiekiama	-	-	No	-	-
58755	72969	1072969	ampulė	2 ml N5		Receptinis	LT/1/14/3523/002	Netiekiama	-	-	No	-	-
58756	72970	1072970	ampulė	2 ml N10		Receptinis	LT/1/14/3523/003	Netiekiama	-	-	No	-	-
58757	72971	1072971	ampulė	2 ml N25		Receptinis	LT/1/14/3523/004	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2018-07-03	Išregistruotas
2014-03-24	Registruotas