Voltaren Emulgel 20mg/g gel for external use

Država: Armenija

Jezik: engleski

Izvor: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Uputa o lijeku Uputa o lijeku (PIL)
11-09-2015
Svojstava lijeka Svojstava lijeka (SPC)
22-08-2018

Aktivni sastojci:

diclofenac (diclofenac diethylamine)

Dostupno od:

Novartis Consumer Health S.A.

ATC koda:

M02AA15

INN (International ime):

diclofenac (diclofenac diethylamine)

Doziranje:

20mg/g

Farmaceutski oblik:

gel for external use

Jedinice u paketu:

50g laminated tube, 100g laminated tube

Tip recepta:

OTC

Status autorizacije:

Registered

Datum autorizacije:

2015-09-04

Svojstava lijeka

                                Novartis Consumer Health SA
CH-1260 Nyon, Switzerland
Global Regulatory Affairs
VOLTAREN ®EMULGEL®
Gel
Diclofenac diethylamine 2.32%
F.AADI01
REGIONAL SUMMARY OF PRODUCT CHARACTERISTICS (SMPC)
Property of Novartis Consumer Health
Confidential
May not be used, divulged, published or otherwise disclosed
without the consent of Novartis Consumer Health
Novartis Consumer Health SA
CONFIDENTIAL
Page 2
EU-rSmPC
Voltaren Forte 2.32% gel
TABLE OF CONTENTS
1
NAME OF THE MEDICINAL PRODUCT
.......................................................................
3
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
............................................. 3
3
PHARMACEUTICAL FORM
............................................................................................
3
4
CLINICAL PARTICULARS
..............................................................................................
3
4.1
Therapeutic indications
............................................................................................
3
4.2
Posology and method of administration
.................................................................. 3
4.3
Contraindications
.....................................................................................................
4
4.4
Special warnings and precautions for use
................................................................ 5
4.5
Interaction with other medicinal products and other forms of
interaction .............. 5
4.6
Pregnancy and lactation
...........................................................................................
5
4.7
Effects on ability to drive and use machines
........................................................... 5
4.8
Undesirable effects
..................................................................................................
5
4.9
Overdose
..................................................................................................................
6
5
PHARMACOLOGICAL PROPERTIES
............................................................................
6
                                
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