Sanoral

Medicinal product

(Invented) name

Sanoral

Active substance (s)

Olmesartanas medoksomilis/Amlodipinas

Strength

40 mg/10 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)

C09DB02, Olmesartan medoxomil and amlodipine

Marketing authorisation holder

Menarini International Operations Luxembourg S.A., Liuksemburgas

Date of authorisation

2008-11-27

Date of renewal

2013-08-13

Documents

1363 Pakuotės lapelis 40mg_10mg 2025 01 17.docx

1363 Sanoral 40_10 PCS PL 2025 01 17.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

10b

Procedure number

NL/H/1115/003/DC

Marketing authorisation procedure

Decentralizuota procedūra

Qualitative and quantitative composition

Tabletėje yra	1 vnt.
Olmesartanas medoksomilis	40 mg
Amlodipinas	10 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
23605	26295	1026295	lizdinė plokštelė	N14		Receptinis	LT/1/08/1363/009	Netiekiama	-	-	No	-	-
23982	26658	1026658	lizdinė plokštelė	N28		Receptinis	LT/1/08/1363/010	Tiekiama	-	-	No	-	-	Download
23983	26659	1026659	lizdinė plokštelė	N56		Receptinis	LT/1/08/1363/011	Netiekiama	-	-	No	-	-
23984	26660	1026660	lizdinė plokštelė	N98		Receptinis	LT/1/08/1363/012	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2013-08-13	Perregistruotas
2008-11-27	Registruotas