Duloxetine Lilly

Medicinal product

(Invented) name

Duloxetine Lilly

Active substance (s)

Duloksetinas

Strength

30 mg

Pharmaceutical form

skrandyje neirios kietosios kapsulės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

N06AX21, Duloxetine

Marketing authorisation holder

Eli Lilly Nederland B.V., Nyderlandai

Date of authorisation

2014-12-08

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

10c

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Hard gastro-resistant capsules	1 vnt.
Duloksetinas	30 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
60902	75208	1075208	lizdinė plokštelė	N7		Receptinis	EU/1/14/972/001	Netiekiama	-	-	No	-	-
60903	75209	1075209	lizdinė plokštelė	N28		Receptinis	EU/1/14/972/002	Netiekiama	-	-	No	-	-
60904	75210	1075210	lizdinė plokštelė	N98		Receptinis	EU/1/14/972/003	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2014-12-08	Registruotas