GABAPENTIN CAPSULES

Land: Kanada

Språk: engelska

Källa: Health Canada

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Produktens egenskaper Produktens egenskaper (SPC)
21-08-2009

Aktiva substanser:

GABAPENTIN

Tillgänglig från:

RANBAXY PHARMACEUTICALS CANADA INC.

ATC-kod:

N02BF01

INN (International namn):

GABAPENTIN

Dos:

400MG

Läkemedelsform:

CAPSULE

Sammansättning:

GABAPENTIN 400MG

Administreringssätt:

ORAL

Enheter i paketet:

30/100/500

Receptbelagda typ:

Prescription

Terapiområde:

MISCELLANEOUS ANTICONVULSANTS

Produktsammanfattning:

Active ingredient group (AIG) number: 0125929002; AHFS:

Bemyndigande status:

CANCELLED PRE MARKET

Tillstånd datum:

2023-07-24

Produktens egenskaper

                                _ _
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_Page 1 of 28_
PRODUCT MONOGRAPH
PR
GABAPENTIN CAPSULES
Gabapentin Capsules USP
100 mg, 300 mg, and 400 mg
Antiepileptic Agent
Ranbaxy Pharmaceuticals Canada Inc., Date of Preparation: August 20,
2009.
2680 Matheson Blvd. E., Suite 200
Mississauga, Ontario
L4W 0A5
Submission Control No: 132106
_ _
_ _
_Page 2 of 28_
TABLE OF CONTENTS
PART I: HEALTH PROFESSIONAL
INFORMATION..............................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL
USE..............................................................................3
CONTRAINDICATIONS
....…...........................................................................................3
WARNINGS AND
PRECAUTIONS..................................................................................3
ADVERSE
REACTIONS....................................................................................................5
DRUG INTERACTIONS
..................................................................................................11
DOSAGE AND
ADMINISTRATION..............................................................................13
OVERDOSAGE
................................................................................................................15
ACTION AND CLINICAL PHARMACOLOGY
............................................................15
STORAGE AND
STABILITY..........................................................................................18
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................18
PART II: SCIENTIFIC INFORMATION
....................................................................20
PHARMACEUTICAL
INFORMATION..........................................................................20
CLINICAL
TRIALS..........................................................................................................21
DETAILED
PHARMACOLOGY..............................................................
                                
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