Fotivda

Medicinal product

(Invented) name

Fotivda

Active substance (s)

Tivozanibas

Strength

890 µg

Pharmaceutical form

kietosios kapsulės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L01EK03, tivozanib

Marketing authorisation holder

Recordati Netherlands B.V., Nyderlandai

Date of authorisation

2017-08-24

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Hard capsule	1 vnt.
Tivozanibas	890 µg

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
97699	83794	1083794	buteliukas	N21		Receptinis	EU/1/17/1215/001	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2017-08-24	Registruotas