FINACEA GEL

Country: Kanada

Lingwa: Ingliż

Sors: Health Canada

Ixtrih issa

Ingredjent attiv:

AZELAIC ACID

Disponibbli minn:

LEO PHARMA INC

Kodiċi ATC:

D10AX03

INN (Isem Internazzjonali):

AZELAIC ACID

Dożaġġ:

15%

Għamla farmaċewtika:

GEL

Kompożizzjoni:

AZELAIC ACID 15%

Rotta amministrattiva:

TOPICAL

Unitajiet fil-pakkett:

15G/50G

Tip ta 'preskrizzjoni:

Prescription

Żona terapewtika:

MISC. SKIN AND MUCOUS MEMBRANE AGENTS

Sommarju tal-prodott:

Active ingredient group (AIG) number: 0126787002; AHFS:

L-istatus ta 'awtorizzazzjoni:

APPROVED

Data ta 'l-awtorizzazzjoni:

2005-09-02

Karatteristiċi tal-prodott

                                _FINACEA Product Monograph, version 1.0_
_Page 1 of 20 _
PRODUCT MONOGRAPH
PR FINACEA
®
Azelaic Acid Gel
15% w/w
Topical
Antirosacea Agent
LEO Pharma Inc.
Thornhill, Ontario
L3T 7W8
www.leo-pharma.ca
Submission Control No.: 229634
Date of Revision:
September 18, 2019
®Registered trademark of LEO Pharma A/S used under license by LEO
Pharma Inc., Thornhill, ON
_FINACEA Product Monograph, version 1.0_
_Page 2 of 20 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
..........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND PRECAUTIONS
..................................................................................3
ADVERSE REACTIONS
....................................................................................................5
DRUG INTERACTIONS
....................................................................................................6
DOSAGE AND ADMINISTRATION
................................................................................7
OVERDOSAGE
..................................................................................................................7
ACTION AND CLINICAL PHARMACOLOGY
..............................................................8
STORAGE AND STABILITY
............................................................................................9
SPECIAL HANDLING INSTRUCTIONS
.........................................................................9
DOSAGE FORMS, COMPOSITION AND PACKAGING
...............................................9
PART II: SCIENTIFIC INFORMATION
...............................................................................10
PHARMACEUTICAL INFORMATION
................................................
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 18-09-2019

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti