NEURONTIN CAPSULE

国: カナダ

言語: 英語

ソース: Health Canada

有効成分:

GABAPENTIN

から入手可能:

BGP PHARMA ULC

ATCコード:

N02BF01

INN（国際名）:

GABAPENTIN

投薬量:

100MG

医薬品形態:

CAPSULE

構図:

GABAPENTIN 100MG

投与経路:

ORAL

パッケージ内のユニット:

100

処方タイプ:

Prescription

治療領域:

MISCELLANEOUS ANTICONVULSANTS

製品概要:

Active ingredient group (AIG) number: 0125929001; AHFS:

認証ステータス:

APPROVED

承認日:

2001-01-05

製品の特徴

_NEURONTIN (gabapentin) _
_Page 1 of 38_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
NEURONTIN®
Gabapentin Capsules
Capsules, 100 mg, 300 mg and 400 mg, oral
Gabapentin Tablets
Tablets, 600 mg and 800 mg, oral
Antiepileptic Agent
BGP Pharma ULC
85 Advance Road
Etobicoke (Ontario)
Canada M8Z 2S6
Date of Initial Approval:
MAY 05, 2023
Date of Revision:
OCTOBER 16, 2023
Submission Control No: 275525
®
Viatris Specialty LLC
BGP Pharma ULC, a Viatris company, Licensee
© BGP Pharma ULC, 2023
_ _
_NEURONTIN (gabapentin) _
_Page 2 of 38_
RECENT MAJOR LABEL CHANGES
7 WARNINGS AND PRECAUTIONS, Dependence/Tolerance
10-2023
7.1 Special Populations, 7.1.1 Pregnant Women, Neonatal
withdrawal syndrome
02-2023
7.1 Special Populations, 7.1.1 Pregnant Women, Women of
childbearing potential/Contraception
10-2023
7.1 Special Populations, 7.1.1 Pregnant Women, Teratogenic
Potential
10-2023
TABLE OF CONTENTS
SECTIONS OR SUBSECTIONS THAT ARE NOT APPLICABLE AT THE TIME OF
AUTHORIZATION ARE NOT LISTED.
RECENT MAJOR LABEL CHANGES
.............................................................................................
2
TABLE OF CONTENTS
...............................................................................................................
2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................
4
1
INDICATIONS
................................................................................................................
4
1.1
Pediatrics
.................................................................................................................
4
1.2
Geriatrics
.................................................................................................................
4
2
CONTRAINDICATIONS
..................................................................................................
4
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
............................................................. 4
4
DOSAGE AND ADMINISTRATION
......................