APO-METHYLPHENIDATE ER TABLET (EXTENDED-RELEASE)

Krajina: Kanada

Jazyk: angličtina

Zdroj: Health Canada

Aktívna zložka:

METHYLPHENIDATE HYDROCHLORIDE

Dostupné z:

APOTEX INC

ATC kód:

N06BA04

INN (Medzinárodný Name):

METHYLPHENIDATE

Dávkovanie:

36MG

Forma lieku:

TABLET (EXTENDED-RELEASE)

Zloženie:

METHYLPHENIDATE HYDROCHLORIDE 36MG

Spôsob podávania:

ORAL

Počet v balení:

100

Typ predpisu:

Schedule G (CDSA III)

Terapeutické oblasti:

Respiratory and CNS Stimulants

Prehľad produktov:

Active ingredient group (AIG) number: 0107548005; AHFS:

Stav Autorizácia:

APPROVED

Dátum Autorizácia:

2016-03-07

Súhrn charakteristických

_APO-METHYLPHENIDATE ER (Methylphenidate Hydrochloride
Extended-Release Tablets) _
_Page 1 of 58_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
APO-METHYLPHENIDATE ER
Methylphenidate Hydrochloride Extended-Release Tablets
Extended-Release Tablets, 18 mg, 27 mg, 36 mg and 54 mg, Oral
Apotex Standard
Central Nervous System Stimulant
Apotex Inc.
150 Signet Drive
Toronto, Ontario
M9L 1T9
Date of Initial Authorization:
FEB 03, 2010
Date of Revision:
JUL 28, 2023
Submission Control Number : 272953
_APO-METHYLPHENIDATE ER (Methylphenidate Hydrochloride
Extended-Release Tablets) _
_Page 2 of 58_
RECENT MAJOR LABEL CHANGES
4 DOSAGE AND ADMINISTRATION, 4.5 Missed Dose
07/2023
7 WARNINGS AND PRECAUTIONS, Neurologic, Serotonin toxicity/Serotonin
syndrome
07/2023
7 WARNINGS AND PRECAUTIONS, Reproductive Health: Female and Male
Potential
07/2023
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
.................................................................................................
5
3
SERIOUS WARNINGS AND PRECAUTIONS BOX
............................................................ 5
4
DOSAGE AND ADMINISTRATION
.........................................................................