Lorista

Medicinal product

(Invented) name

Lorista

Active substance (s)

Losartano kalio druska

Strength

50 mg

Pharmaceutical form

plėvele dengtos tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

C09CA01, Losartan

Marketing authorisation holder

KRKA, d.d., Novo mesto, Slovėnija

Date of authorisation

2001-10-08

Date of renewal

2012-06-15

Documents

2983 Pakuotės lapelis 2025 05 22.docx

2983 Lorista 50mg tab RPP 2025 05 22.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

Marketing authorisation procedure

Nacionalinė procedūra

Qualitative and quantitative composition

Tabletėje yra	1 vnt.
Losartano kalio druska	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
1746	4320	1004320	lizdinė plokštelė	N28		Receptinis	LT/1/01/2983/001	Tiekiama	-	-	No	-	-	Download
17342	21235	1021235	lizdinė plokštelė	N56		Receptinis	LT/1/01/2983/002	Netiekiama	-	-	No	-	-
17343	21236	1021236	lizdinė plokštelė	N84		Receptinis	LT/1/01/2983/003	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2012-06-15	Perregistruotas
2001-10-08	Registruotas