IBUPROFEN AND PSEUDOEPHEDRINE TABLET

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktívna zložka:

IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

Dostupné z:

MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC

ATC kód:

M01AE51

INN (Medzinárodný Name):

IBUPROFEN, COMBINATIONS

Dávkovanie:

200MG; 30MG

Forma lieku:

TABLET

Zloženie:

IBUPROFEN 200MG; PSEUDOEPHEDRINE HYDROCHLORIDE 30MG

Spôsob podávania:

ORAL

Počet v balení:

20/40

Typ predpisu:

OTC

Terapeutické oblasti:

ALPHA-AND BETA-ADRENERGIC AGONISTS

Prehľad produktov:

Active ingredient group (AIG) number: 0222394001; AHFS:

Stav Autorizácia:

CANCELLED POST MARKET

Dátum Autorizácia:

2016-01-22

Súhrn charakteristických

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PRODUCT MONOGRAPH
IBUPROFEN AND PSEUDOEPHEDRINE
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
TABLETS
USP
200MG & 30 MG
Therapeutic Classification
ANALGESIC/ANTIPYRETIC/NASAL DECONGESTANT
McNeil Consumer Healthcare
88 McNabb Street
Markham, Ontario L3R 5L2
Date of Preparation:
January 18, 2007
Control # 111161
© McNeil Consumer Healthcare 2006
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TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL
USE..............................................................................3
CONTRAINDICATIONS
...................................................................................................3
WARNINGS AND
PRECAUTIONS..................................................................................4
ADVERSE
REACTIONS....................................................................................................7
DRUG INTERACTIONS
..................................................................................................10
DOSAGE AND
ADMINISTRATION..............................................................................12
OVERDOSAGE
................................................................................................................13
ACTION AND CLINICAL PHARMACOLOGY
............................................................13
STORAGE AND
STABILITY..........................................................................................16
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................16
PART II: SCIENTIFIC INFORMATION
...............................................................................17
PHARMACEUTICAL
INFORMATION..........................................................................17
CLINICAL
TRIALS..........................................................................................................18
DETAILED