Approval · Notice of Compliance 35787 · 2025
VENCLEXTA: Notice of Compliance 35787
Issued July 31, 2025
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
- 35787
- Date
- July 31, 2025
- Company
- AbbVie CorporationSaint-Laurent, Quebec, Canada
- Product type
- Prescription Pharmaceutical
- Submission
- Supplement to a New Drug Submission (SNDS), supplement
- Submission class
- Other
- Reason
- Addition of new indication: VENCLEXTA, in combination with ibrutinib, is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (MCL)
Products in this notice
| Brand | DIN | Status today |
|---|---|---|
| VENCLEXTA | Not yet assigned | — |
Medicinal ingredients
- VENETOCLAX 10 MG per TAB
- VENETOCLAX 50 MG per TAB
- VENETOCLAX 100 MG per TAB