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:
Cancelled Pre Market
Current status date:
2020-04-27
Original market date: See footnote 1
Product name:
ACT GEMCITABINE
DIN:
02436191
Product Monograph/Veterinary Labelling:
Date:
2014-12-31
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
ACTAVIS PHARMA COMPANY
30 Novopharm Court
Toronto
Ontario
Canada
M1B 2K9
Class:
Human
Dosage form(s):
Powder For Solution
Route(s) of administration:
Intravenous
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
10:00.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
L01BC05 GEMCITABINE
Active ingredient group (AIG) number:See footnote5
0133122001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| GEMCITABINE (GEMCITABINE HYDROCHLORIDE) | 200 MG / VIAL |