Cymbalta

Medicinal product

(Invented) name

Cymbalta

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

2004-02-12

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

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
25758	4485	1004485	lizdinė plokštelė	N28		Receptinis	EU/1/04/296/001	Netiekiama	2025-05-02	-	No	-	-
25759	28355	1028355	lizdinė plokštelė	N7		Receptinis	EU/1/04/296/006	Netiekiama	-	-	No	-	-
25766	28361	1028361	lizdinė plokštelė	N98		Receptinis	EU/1/04/296/009	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2004-02-12	Registruotas