Approval · Notice of Compliance 16695 · 2015
TEVA-RISPERIDONE: Notice of Compliance 16695
Issued March 16, 2015
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
- 16695
- Date
- March 16, 2015
- Company
- Teva Canada LimitedToronto, Ontario, Canada
- Product type
- Prescription Pharmaceutical
- Submission
- Supplement to an Abbreviated New Drug Submission (SANDS), supplement
- Submission class
- Other
- Reason
- Revision to the indications
- Therapeutic class
- Antipsychotic agent
- Canadian reference product
- RISPERDAL (Janssen Inc.)
Products in this notice
| Brand | DIN | Status today |
|---|---|---|
| TEVA-RISPERIDONE | Not yet assigned | — |
Medicinal ingredients
- RISPERIDONE 0.25 MG per TAB
- RISPERIDONE 0.5 MG per TAB
- RISPERIDONE 1 MG per TAB
- RISPERIDONE 2 MG per TAB
- RISPERIDONE 3 MG per TAB
- RISPERIDONE 4 MG per TAB