Approval · Notice of Compliance 21899 · 2019
SUNPHARMA FENOFIBRATE E: Notice of Compliance 21899
Issued February 26, 2019
A Notice of Compliance is Health Canada’s approval of a drug submission: a new drug, a new use or form, or a change to an approved one. The product itself is in the Drug Product Database, with its current status.
- Notice number
- 21899
- Date
- February 26, 2019
- Company
- Sun Pharma Canada Inc.Brampton, Ontario, Canada
- Product type
- Prescription Pharmaceutical
- Submission
- Abbreviated New Drug Submission (ANDS)
- Submission class
- Labelling Only
- Reason
- Manufacturer and prodeuct name change. revisions to the labelling
- Canadian reference product
- LIPIDIL EZ (Fournier Pharma Inc)
Products in this notice
| Brand | DIN | Status today |
|---|---|---|
| SUNPHARMA FENOFIBRATE E | 02454696 | Marketed |
Medicinal ingredients
- FENOFIBRATE 145 MG per TAB