Approval · Notice of Compliance 38431 · 2026
ACTONEL: Notice of Compliance 38431
Issued October 8, 2026
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
- 38431
- Date
- October 8, 2026
- Company
- AbbVie CorporationSaint-Laurent, Quebec, Canada
- Product type
- Prescription Pharmaceutical
- Submission
- Supplement to a New Drug Submission (SNDS), supplement
- Submission class
- Other
- Reason
- Update to the Product Monograph with new safety information. Product Monograph reformatted to the Master Template. Update to Patient Medication Information
Products in this notice
| Brand | DIN | Status today |
|---|---|---|
| ACTONEL | Not yet assigned | — |
| ACTONEL DR | Not yet assigned | — |
Medicinal ingredients
- RISEDRONATE SODIUM HEMI-PENTAHYDRATE 35 MG per TAB
- RISEDRONATE SODIUM HEMI-PENTAHYDRATE 150 MG per TAB