Voltaren Emulgel 20mg/g gel for external use

Land: Armenië

Taal: Engels

Bron: Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

Bijsluiter Bijsluiter (PIL)
11-09-2015
Productkenmerken Productkenmerken (SPC)
22-08-2018

Werkstoffen:

diclofenac (diclofenac diethylamine)

Beschikbaar vanaf:

Novartis Consumer Health S.A.

ATC-code:

M02AA15

INN (Algemene Internationale Benaming):

diclofenac (diclofenac diethylamine)

Dosering:

20mg/g

farmaceutische vorm:

gel for external use

Eenheden in pakket:

50g laminated tube, 100g laminated tube

Prescription-type:

OTC

Autorisatie-status:

Registered

Autorisatie datum:

2015-09-04

Productkenmerken

                                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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Documenten in andere talen

Bijsluiter Bijsluiter Russisch 22-08-2018

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