Product information
From Health Canada
The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.
Current status:
Marketed
Current status date:
2023-02-01
Original market date: See footnote 1
2023-02-01
Product name:
PRO-SITAGLIPTIN MALATE / METFORMIN HYDROCHLORIDE
DIN:
02534231
Product Monograph/Veterinary Labelling:
Date:
2023-01-09
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
PRO DOC LIMITEE
2925 Boulevard Industriel
Laval
Quebec
Canada
H7L 3W9
Class:
Human
Dosage form(s):
Tablet
Route(s) of administration:
Oral
Number of active ingredient(s):
2
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
68:20.05 , 68:20.04
Anatomical Therapeutic Chemical (ATC): See footnote 4
A10BD07 METFORMIN AND SITAGLIPTIN
Active ingredient group (AIG) number:See footnote5
0252656002
Active ingredient(s) See footnote8 | Strength |
---|---|
METFORMIN HYDROCHLORIDE | 850 MG |
SITAGLIPTIN (SITAGLIPTIN MALATE) | 50 MG |