IMODIUM LIQUI-GELS CAPSULE

Quốc gia: Canada

Ngôn ngữ: Tiếng Anh

Nguồn: Health Canada

Thành phần hoạt chất:

LOPERAMIDE HYDROCHLORIDE

Sẵn có từ:

MCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC

Mã ATC:

A07DA03

INN (Tên quốc tế):

LOPERAMIDE

Liều dùng:

2MG

Dạng dược phẩm:

CAPSULE

Thành phần:

LOPERAMIDE HYDROCHLORIDE 2MG

Tuyến hành chính:

ORAL

Các đơn vị trong gói:

6/12/18/24/36/42

Loại thuốc theo toa:

OTC

Khu trị liệu:

ANTIDIARRHEA AGENTS

Tóm tắt sản phẩm:

Active ingredient group (AIG) number: 0111332001; AHFS:

Tình trạng ủy quyền:

APPROVED

Ngày ủy quyền:

2011-11-14

Đặc tính sản phẩm

_Product Monograph Master Template _
_Template Date: September 2020 _
_IMODIUM_
®
_Quick Dissolve, Loperamide Hydrochloride Tablets _
_IMODIUM_
®
_Calming Liquid, Loperamide Hydrochloride Oral Solution _
_IMODIUM_
®
_ LIQUI-GELS_
®
_, Loperamide Hydrochloride Capsules _
_Page 1 of 40_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
IMODIUM
® QUICK DISSOLVE
Loperamide Hydrochloride Tablets
Tablet (Orally Disintegrating), 2 mg, Oral
McNeil Std
and
IMODIUM
®
CALMING LIQUID
Loperamide Hydrochloride Oral Solution
Solution, 2 mg / 15 mL, Oral
McNeil Std
and
IMODIUM
® LIQUI-GELS
®
Loperamide Hydrochloride Capsules,
Capsule, 2 mg, Oral
McNeil Std
Antidiarrheal agent
McNeil Consumer Healthcare,
Division of Johnson & Johnson Inc.
88 McNabb Street
Markham, Ontario
L3R 5L2
Date of Initial Authorization:
IMODIUM
®
Quick Dissolve:
January 15, 1997
IMODIUM
®
Calming Liquid:
February 07, 2007
IMODIUM
®
LIQUI-GELS
®
:
November 10, 2011
Date of Revision:
December 2, 2022
Submission Control Number: 265788
LIQUI-GELS
®
is a registered trademark of Catalent Pharma Solutions, Inc., used
under license
_ _
_Product Monograph Master Template _
_Template Date: September 2020 _
_IMODIUM_
®
_Quick Dissolve, Loperamide Hydrochloride Tablets _
_IMODIUM_
®
_Calming Liquid, Loperamide Hydrochloride Oral Solution _
_IMODIUM_
®
_ LIQUI-GELS_
®
_, Loperamide Hydrochloride Capsules _
_Page 2 of 40_
RECENT MAJOR LABEL CHANGES
Section 4: Dosage and Administration – Addition of drug
withdrawal syndrome
Section 5: Overdosage – Addition of drug withdrawal
syndrome
Section 7: Warnings and Precautions – Addition of drug
withdrawal syndrome
Section 14: Clinical Trials – Addition of drug withdrawal
syndrome
06/2022
06/2022
06/2022
06/2022
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 ...................................................