MOTRIMAX 12 HOUR TABLETS

Nazione: Canada

Lingua: inglese

Fonte: Health Canada

Principio attivo:

NAPROXEN SODIUM

Commercializzato da:

MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC

Codice ATC:

M01AE02

INN (Nome Internazionale):

NAPROXEN

Dosaggio:

220MG

Forma farmaceutica:

TABLET

Composizione:

NAPROXEN SODIUM 220MG

Via di somministrazione:

ORAL

Confezione:

24/50/100/120/200/300/400

Tipo di ricetta:

OTC

Area terapeutica:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

Dettagli prodotto:

Active ingredient group (AIG) number: 0113934003; AHFS:

Stato dell'autorizzazione:

APPROVED

Data dell'autorizzazione:

2016-01-29

Scheda tecnica

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_MotriMAX 12 HOUR™ Tablets Product Monograph _
_Page 1 of 32_
PRODUCT MONOGRAPH
MOTRIMAX 12 HOUR™ TABLETS
Naproxen Sodium Tablets USP
220 mg Tablets and Caplets
Non-steroidal anti-inflammatory drug
Analgesic, Antipyretic
McNeil Consumer Healthcare
Division of Johnson & Johnson Inc.
88 McNabb St.
Markham, Ontario
L3R 5L2
Date of Preparation:
January 28, 2016
Control No: 191125
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_MotriMAX 12 HOUR™ Tablets Product Monograph _
_Page 2 of 32_
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
...................................................................................................
6
DRUG INTERACTIONS
...................................................................................................
9
DOSAGE AND ADMINISTRATION
.............................................................................
11
OVERDOSAGE
...............................................................................................................
12
ACTION AND CLINICAL PHARMACOLOGY
........................................................... 12
STORAGE AND STABILITY
.........................................................................................
14
DOSAGE FORMS, COMPOSITION AND PACKAGING
............................................ 14
PART II: SCIENTIFIC INFORMATION
..............................................................................
15
PHARMACEUTICAL INFORMATION
.........................................................................
15
CLINICAL TRIALS
...............................