Approval · Notice of Compliance 8300 · 2006
RANITIDINE: Notice of Compliance 8300
Issued October 2, 2006
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
- 8300
- Date
- October 2, 2006
- Company
- Genpharm Inc.Etobicoke, Ontario, Canada
- Product type
- Prescription Pharmaceutical
- Submission
- New Drug Submission (NDS)
- Submission class
- Admin
- Reason
- Additional product name
- Therapeutic class
- Histamine h2-receptor antagonist
Products in this notice
| Brand | DIN | Status today |
|---|---|---|
| RANITIDINE | 02286106 | Cancelled Post Market |
| RANITIDINE | 02286114 | Cancelled Post Market |
Medicinal ingredients
- RANITIDINE HCL 150 MG per TAB
- RANITIDINE HCL 300 MG per TAB