SANDOZ FENOFIBRATE E TABLET

Страна: Канада

мова: англійська

Джерело: Health Canada

Активний інгредієнт:

FENOFIBRATE

Доступна з:

SANDOZ CANADA INCORPORATED

Код атс:

C10AB05

ІПН (Міжнародна Ім'я):

FENOFIBRATE

Дозування:

145.0MG

Фармацевтична форма:

TABLET

Склад:

FENOFIBRATE 145.0MG

Адміністрація маршрут:

ORAL

Одиниць в упаковці:

30

Тип рецепту:

Prescription

Терапевтична области:

FRIBIC ACID DERIVATIVES

Огляд продуктів:

Active ingredient group (AIG) number: 0118895006; AHFS:

Статус Авторизація:

APPROVED

Дата Авторизація:

2012-08-02

Характеристики продукта

_Sandoz Fenofibrate E Page 1 of 43_
PRODUCT MONOGRAPH
PR
SANDOZ FENOFIBRATE E
Fenofibrate tablets
48 mg and 145 mg
Manufacturer’s standard
Lipid Metabolism Regulator
Sandoz Canada Inc. Date of Revision: November 17, 2017
145 Jules-Léger
Boucherville, QC, Canada
J4B 7K8
Submission Control No: 204109
_ _
_Sandoz Fenofibrate E Page 2 of 43_
TABLE OF CONTENTS
PART 1: HEALTH PROFESSIONAL INFORMATION
.........................................................3
SUMMARY PRODUCT INFORMATION
........................................................................3
INDICATIONS AND CLINICAL USE
..............................................................................3
CONTRAINDICATIONS
...................................................................................................4
WARNINGS AND PRECAUTIONS
..................................................................................4
ADVERSE REACTIONS
....................................................................................................9
DRUG INTERACTIONS
..................................................................................................13
DOSAGE AND ADMINISTRATION
..............................................................................17
OVERDOSAGE
................................................................................................................18
ACTION AND CLINICAL PHARMACOLOGY
............................................................18
STORAGE AND STABILITY
..........................................................................................20
DOSAGE FORMS, COMPOSITION AND PACKAGING
.............................................20
PART II: SCIENTIFIC INFORMATION
................................................................................22
PHARMACEUTICAL INFORMATION
..........................................................................22
CLINICAL TRIALS
..........................................................................................................23
DETAILED PHARMACOLOGY
............