Temozolomide Teva

Medicinal product

(Invented) name

Temozolomide Teva

Active substance (s)

Temozolomidas

Strength

20 mg

Pharmaceutical form

kietosios kapsulės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L01AX03, Temozolomide

Marketing authorisation holder

Teva B.V., Nyderlandai

Date of authorisation

2010-01-28

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Capsule, hard	1 vnt.
Temozolomidas	20 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
39303	53002	1053002	buteliukas	N5		Receptinis	EU/1/09/606/003	Netiekiama	2024-10-30	-	No	-	-
39304	53003	1053003	buteliukas	N20		Receptinis	EU/1/09/606/004	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2010-01-28	Registruotas