ANALGESIC AND MUSCLE RELAXANT CAPLETS TABLET

Land: Kanada

Sprache: Englisch

Quelle: Health Canada

Kaufe es jetzt

Fachinformation Fachinformation (SPC)
09-01-2013

Wirkstoff:

IBUPROFEN; METHOCARBAMOL

Verfügbar ab:

TEVA CANADA LIMITED

ATC-Code:

M03BA53

INN (Internationale Bezeichnung):

METHOCARBAMOL, COMBINATIONS EXCL PSYCHOLEPTICS

Dosierung:

200MG; 500MG

Darreichungsform:

TABLET

Zusammensetzung:

IBUPROFEN 200MG; METHOCARBAMOL 500MG

Verabreichungsweg:

ORAL

Einheiten im Paket:

18/40

Verschreibungstyp:

OTC

Therapiebereich:

CENTRALLY ACTING SKELETAL MUSCLE RELAXANTS

Produktbesonderheiten:

Active ingredient group (AIG) number: 0248961001; AHFS:

Berechtigungsstatus:

CANCELLED POST MARKET

Berechtigungsdatum:

2021-08-12

Fachinformation

                                1 | P a g e
PRODUCT MONOGRAPH
ANALGESIC & MUSCLE RELAXANT CAPLETS
500 MG METHOCARBAMOL AND 200 MG IBUPROFEN TABLETS
THERAPEUTIC CLASSIFICATION
MUSCLE RELAXANT / ANALGESIC
TEVA CANADA LIMITED
Date of Preparation:
30 Novopharm Court
January 8, 2013
Toronto, Canada
M1B 2K9
Control# 161025
2 | P a g e
TABLE OF CONTENTS
Clinical Pharmacology
..............................................................................................................................
3
Indications:
................................................................................................................................................
7
Contraindications
......................................................................................................................................
8
Warnings:
..................................................................................................................................................
8
Precautions
..............................................................................................................................................
12
Drug Interactions
....................................................................................................................................
13
Adverse Reactions
..................................................................................................................................
15
Symptoms and Treatment of Overdose
...................................................................................................
17
Dosage and
Administration.....................................................................................................................
18
Pharmaceutical Information
....................................................................................................................
19
Composition:
...........................................................................................................................................
21
Availability of Dosage Forms
..........................
                                
                                Lesen Sie das vollständige Dokument