Rubraca

Medicinal product

(Invented) name

Rubraca

Active substance (s)

Rukaparibas

Strength

250 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)

L01XK03, rucaparib

Marketing authorisation holder

pharmaand GmbH, Austrija

Date of authorisation

2018-05-24

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

Film-coated tablet	1 vnt.
Rukaparibas	250 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
99642	85749	1085749	buteliukas	N60		Receptinis	EU/1/17/1250/002	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2018-05-24	Registruotas