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:
2012-03-05
Original market date: See footnote 1
1965-12-31
Product name:
PHENOBARB ELIXIR
DIN:
00645575
Product Monograph/Veterinary Labelling:
Date:
2020-10-02
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
PENDOPHARM DIVISION OF PHARMASCIENCE INC
100
6111 Royalmount Ave
Montreal
Quebec
Canada
H4P 2T4
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Schedule G (CDSA IV)
American Hospital Formulary Service (AHFS): See footnote 3
28:12.04 , 28:24.04
Anatomical Therapeutic Chemical (ATC): See footnote 4
N03AA02 PHENOBARBITAL
Active ingredient group (AIG) number:See footnote5
0105950008
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| PHENOBARBITAL | 5 MG / ML |