ACH-SITAGLIPTIN TABLET

Ország: Kanada

Nyelv: angol

Forrás: Health Canada

Aktív összetevők:

SITAGLIPTIN (SITAGLIPTIN PHOSPHATE)

Beszerezhető a:

ACCORD HEALTHCARE INC

ATC-kód:

A10BH01

INN (nemzetközi neve):

SITAGLIPTIN

Adagolás:

50MG

Gyógyszerészeti forma:

TABLET

Összetétel:

SITAGLIPTIN (SITAGLIPTIN PHOSPHATE) 50MG

Az alkalmazás módja:

ORAL

db csomag:

15G/50G

Recept típusa:

Prescription

Termék összefoglaló:

Active ingredient group (AIG) number: 0152414003; AHFS:

Engedélyezési státusz:

APPROVED

Engedély dátuma:

2023-01-05

Termékjellemzők

_ _
_Product Monograph - ACH-SITAGLIPTIN _
_Page 1 of 57_
PRODUCT MONOGRAPH
INCLUDING PATIENT MEDICATION INFORMATION
PR
ACH-SITAGLIPTIN
sitagliptin tablets
Tablets, 25, 50 and 100 mg sitagliptin (as sitagliptin phosphate
anhydrous), Oral
House Standard
ATC Code: A10BH01
Dipeptidyl peptidase 4 (DPP-4) inhibitors
Accord Healthcare Inc.
3535 boul. St. Charles, Suite 704
Kirkland, QC, H9H 5B9
Canada
Date of Initial Authorization:
February 15, 2021
Date of Revision:
September 22, 2022
Submission Control Number: 263618
_Product Monograph - ACH-SITAGLIPTIN Page _2_ of _57
RECENT MAJOR LABEL CHANGES
1 Indications
09/2022
4 Dosage and Administration
09/2022
7 Warnings and Precautions
09/2022
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
................................................................................................................2
PART I: HEALTH PROFESSIONAL INFORMATION
.......................................................................4
1
INDICATIONS
................................................................................................................4
1.1
Pediatrics
...........................................................................................................
4
1.2
Geriatrics............................................................................................................
4
2
CONTRAINDICA TIONS
...................................................................................................4
4
DOSAGE AND ADMINISTRATION
..................................................................................4
4.1
Dosing Considerations
........................................................................................
4
4.2
Recommended Dose and Dosage
Adjustment...................................................... 5
4.4
Administration................................