Voltaren Emulgel 20mg/g gel for external use

Land: Armenien

Sprog: engelsk

Kilde: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Indlægsseddel Indlægsseddel (PIL)
11-09-2015
Produktets egenskaber Produktets egenskaber (SPC)
22-08-2018

Aktiv bestanddel:

diclofenac (diclofenac diethylamine)

Tilgængelig fra:

Novartis Consumer Health S.A.

ATC-kode:

M02AA15

INN (International Name):

diclofenac (diclofenac diethylamine)

Dosering:

20mg/g

Lægemiddelform:

gel for external use

Enheder i pakken:

50g laminated tube, 100g laminated tube

Recept type:

OTC

Autorisation status:

Registered

Autorisation dato:

2015-09-04

Produktets egenskaber

                                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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Indlægsseddel Indlægsseddel russisk 22-08-2018

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