Product information
From Health Canada
No match found
No other product was found with the same active ingredient group.
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:
Cancelled (Unreturned Annual)
Current status date:
2021-12-20
Original market date: See footnote 1
1980-12-31
Product name:
SANOREX
DIN:
00432407
Product Monograph/Veterinary Labelling:
Date:
2015-07-07
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
HEXIM PHARMACEUTICALS INC
600 Meadowlands Parkway, Suite 149
Secaucus
New Jersey
United States
07094
Class:
Human
Dosage form(s):
Tablet
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Targeted (CDSA IV)
American Hospital Formulary Service (AHFS): See footnote 3
28:20.92
Anatomical Therapeutic Chemical (ATC): See footnote 4
A08AA05 MAZINDOL
Active ingredient group (AIG) number:See footnote5
0109331001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| MAZINDOL | 1 MG |