RAN-CARVEDILOL TABLET

Riik: Kanada

keel: inglise

Allikas: Health Canada

Toimeaine:

CARVEDILOL

Saadav alates:

RANBAXY PHARMACEUTICALS CANADA INC.

ATC kood:

C07AG02

INN (Rahvusvaheline Nimetus):

CARVEDILOL

Annus:

3.125MG

Ravimvorm:

TABLET

Koostis:

CARVEDILOL 3.125MG

Manustamisviis:

ORAL

Ühikuid pakis:

100

Retsepti tüüp:

Prescription

Terapeutiline ala:

BETA-ADRENERGIC BLOCKING AGENTS

Toote kokkuvõte:

Active ingredient group (AIG) number: 0122683003; AHFS:

Volitamisolek:

CANCELLED POST MARKET

Loa andmise kuupäev:

2022-09-16

Toote omadused

PRODUCT MONOGRAPH
PR
RAN™-CARVEDILOL
Carvedilol Tablets, House Standard
3.125, 6.25, 12.5 and 25 mg
CONGESTIVE HEART FAILURE AGENT
Ranbaxy Pharmaceuticals Canada Inc. DATE OF REVISION:
126 East Drive SEPTEMBER 14, 2016
Brampton, Ontario
L4W 0A5
Submission Control No: 197425
RAN trademark owned by Sun Pharmaceutical Industries Ltd.
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_RAN-CARVEDILOL Product Monograph _
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_Page 2 of 38 _
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
.............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
....................................................................................................9
DRUG INTERACTIONS
..................................................................................................15
DOSAGE AND ADMINISTRATION
..............................................................................17
OVERDOSAGE
................................................................................................................19
ACTION AND CLINICAL PHARMACOLOGY
............................................................20
STORAGE AND STABILITY
..........................................................................................23
DOSAGE FORMS, COMPOSITION AND PACKAGING
..............................................23
PART II: SCIENTIFIC INFORMATION
...............................................................................25
PHARMACEUTICAL INFORMATION
..........................................................................25
CLINICAL TRIALS
.............................................................................................