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:
2022-02-24
Original market date: See footnote 1
2022-02-24
Product name:
REXXOLIDE
DIN:
02518236
Product Monograph/Veterinary Labelling:
Date:
2021-07-21
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
DECHRA REGULATORY BV
Handelsweg 25
Bladel
--
Netherlands
5531 AE
Class:
Veterinary
Species:
Cattle , Swine (pigs) , Sheep
Dosage form(s):
Solution
Route(s) of administration:
Intramuscular , Subcutaneous
Number of active ingredient(s):
1
Schedule(s):
Prescription
American Hospital Formulary Service (AHFS): See footnote 3
Anatomical Therapeutic Chemical (ATC): See footnote 4
Not Applicable
Active ingredient group (AIG) number:See footnote5
0151667001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| TULATHROMYCIN | 100 MG / ML |