Kengrexal

Medicinal product

(Invented) name

Kengrexal

Active substance (s)

Kangreloras

Strength

50 mg

Pharmaceutical form

milteliai injekcinio ar infuzinio tirpalo koncentratui

Route (s) of administration

leisti į veną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

B01AC25, Cangrelor

Marketing authorisation holder

Chiesi Farmaceutici S.p.A., Italija

Date of authorisation

2015-03-23

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

Powder for concentrate for solution for injection / infusion	1 vnt.
Kangreloras	50 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
61702	76044	1076044	flakonas	N10		Receptinis	EU/1/15/994/001	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2015-03-23	Registruotas