Diclofenac sodium Eletis

Medicinal product

(Invented) name

Diclofenac sodium Eletis

Active substance (s)

Diklofenako natrio druska

Strength

75 mg/3 ml

Pharmaceutical form

injekcinis ar infuzinis tirpalas

Route (s) of administration

leisti į veną, leisti į raumenis

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

M01AB05, Diclofenac

Marketing authorisation holder

UAB Eletis Pharma, Lietuva

Date of authorisation

2025-09-26

Date of renewal

Documents

5863 Diclofenac_Na_Eletis.docx

5863 pakuotes lapelis_2025-09-26.docx

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

Marketing authorisation procedure

Nacionalinė procedūra

Qualitative and quantitative composition

Ampulėje (3 ml tirpalo) yra	3 ml
Diklofenako natrio druska	75 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
118747	104853	1104853	ampulė	3 ml N5		Receptinis	LT/1/25/5863/001	Netiekiama	-	-	No	-	-
118748	104854	1104854	ampulė	3 ml N10		Receptinis	LT/1/25/5863/002	Netiekiama	-	-	No	-	-
118749	104855	1104855	ampulė	3 ml N25		Receptinis	LT/1/25/5863/003	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2025-09-26	Registruotas