MOTRIN CAPLET TABLET

Country: Կանադա

language: անգլերեն

source: Health Canada

active_ingredient:

IBUPROFEN

MAH:

MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC

ATC_code:

M01AE01

INN:

IBUPROFEN

dosage:

200MG

pharmaceutical_form:

TABLET

composition:

IBUPROFEN 200MG

administration_route:

ORAL

units_in_package:

24/50

prescription_type:

OTC

therapeutic_area:

OTHER NONSTEROIDAL ANTIIMFLAMMATORY AGENTS

leaflet_short:

Active ingredient group (AIG) number: 0108883004; AHFS:

authorization_status:

CANCELLED POST MARKET

authorization_date:

2016-01-22

SPC

PRODUCT MONOGRAPH
MOTRIN
®
200 mg
Ibuprofen Tablets USP, 200 mg
MOTRIN
®
Caplet
Ibuprofen Tablets USP, 200 mg
MOTRIN
®
Gelcaps
Ibuprofen Tablets USP, 200 mg
MOTRIN
®
300 mg
Ibuprofen Tablets USP, 300 mg
MOTRIN
®
400 mg
Ibuprofen Tablets USP, 400 mg
Non-Steroidal Anti-inflammatory Drug
Analgesic, Antipyretic Agent
McNeil Consumer Healthcare
Division of Johnson & Johnson Inc.
88 McNabb Street
Markham, Canada
L3R 5L2
Date of Preparation:
May 10, 2002
Date of Revision:
February 26, 2015
Control # 181377
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_Page 2 of 41_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................5
ADVERSE REACTIONS
..................................................................................................11
DRUG INTERACTIONS
..................................................................................................15
DOSAGE AND ADMINISTRATION
..............................................................................17
OVERDOSAGE
................................................................................................................18
ACTION AND CLINICAL PHARMACOLOGY
............................................................19
STORAGE AND STABILITY
..........................................................................................21
SPECIAL HANDLING INSTRUCTIONS
.......................................................................21
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................21
PART II: SCIENTIFIC INFORMATION
.........................................................