Zofenopril e Idroclorotiazide EG

Medicinal product

(Invented) name

Zofenopril e Idroclorotiazide EG

Active substance (s)

Zofenoprilio kalcio druska/Hidrochlorotiazidas

Strength

30 mg/12,5 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)

C09BA15, Zofenopril and diuretics

Marketing authorisation holder

UAB Niromed, Lietuva

Date of authorisation

2025-03-13

Date of renewal

Documents

2420_Zofenopril e Idroclorotiazide EG 30mg-12,5mg_pl_deng_tab_PL_2025-03-13.docx

2420_Zofenopril e Idroclorotiazide EG 30mg-12,5mg_pl_deng_tab_PZ_2025-03-13.docx

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

Procedure number

Marketing authorisation procedure

Lygiagretus importas

Qualitative and quantitative composition

Tabletėje yra:	1 vnt.
Zofenoprilio kalcio druska	30 mg
Hidrochlorotiazidas	12,5 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
116971	103074	1103074	lizdinė plokštelė	N28		Receptinis	LT/L/25/2420/001	Netiekiama	-	-	No	-	-	Download

Stadijos

Data	Stadija
2025-03-13	Registruotas