Bonefurbit

Medicinal product

(Invented) name

Bonefurbit

Active substance (s)

Ibandrono rūgštis

Strength

150 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)

M05BA06, Ibandronic acid

Marketing authorisation holder

UAB Orivas, Lietuva

Date of authorisation

2011-03-30

Date of renewal

2016-05-10

Documents

2391 Bonefurbit PCS PL 2023 02 06.docx

2391 Pakuotės lapelis 2023 02 06.docx

Stage

Perregistruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

NO/H/0153/001/DC

Marketing authorisation procedure

Decentralizuota procedūra

Qualitative and quantitative composition

Tabletėje yra	1 vnt.
Ibandrono rūgštis	150 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
33031	35411	1035411	lizdinė plokštelė	N1		Receptinis	LT/1/11/2391/001	Netiekiama	-	-	No	-	-
45896	59700	1059700	lizdinė plokštelė	N3		Receptinis	LT/1/11/2391/002	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2016-05-10	Perregistruotas
2011-03-30	Registruotas