Integrilin

Medicinal product

(Invented) name

Integrilin

Active substance (s)

Eptifibatidas

Strength

0,75 mg/ml

Pharmaceutical form

infuzinis tirpalas

Route (s) of administration

leisti į veną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

B01AC16, Eptifibatide

Marketing authorisation holder

GlaxoSmithKline (Ireland) Limited , Airija

Date of authorisation

1999-07-01

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

Solution for infusion	1 ml
Eptifibatidas	0,75 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
25859	28451	1028451	flakonas	100 ml, N1		Receptinis	EU/1/99/109/001	Tiekiama	-	2025-12-31	No	-	-

Stadijos

Data	Stadija
1999-07-01	Registruotas