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:
2023-10-04
Original market date: See footnote 1
2023-10-04
Product name:
XYWAV
Description:
0.5 G/ML OF TOTAL SALTS
DIN:
02538237
Product Monograph/Veterinary Labelling:
Date:
2024-07-24
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
JAZZ PHARMACEUTICALS IRELAND LIMITED
5th Floor, Waterloo Exchange, Waterloo Rd.
Dublin
Dublin
Ireland
D04 E5W7
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Oral
Number of active ingredient(s):
4
Schedule(s):
Schedule G (CDSA I)
American Hospital Formulary Service (AHFS): See footnote 3
28:92.00
Anatomical Therapeutic Chemical (ATC): See footnote 4
N07XX04 HYDROXYBUTYRIC ACID
Active ingredient group (AIG) number:See footnote5
0464702001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| CALCIUM OXYBATE | 0.234 G / ML |
| MAGNESIUM OXYBATE | 0.096 G / ML |
| POTASSIUM OXYBATE | 0.13 G / ML |
| SODIUM OXYBATE | 0.04 G / ML |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
| Additional Risk Minimization Measures |
|---|
| Healthcare Professional Education |
| Controlled Distribution Program |
| Patient Consent |
| Patient Education |