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:
Approved
Current status date:
2023-11-02
Product name:
JAMP KETOTIFEN OPHTHALMIC
DIN:
02542722
Product Monograph/Veterinary Labelling:
Date:
2023-10-26
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
JAMP PHARMA CORPORATION
1310 Rue Nobel
Boucherville
Quebec
Canada
J4B 5H3
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Ophthalmic
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
52:02.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
S01GX08 KETOTIFEN
Active ingredient group (AIG) number:See footnote5
0115676003
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| KETOTIFEN (KETOTIFEN FUMARATE) | 0.25 MG / ML |