CALCIMAR DIN 01926691
Status: Marketed
Holder: SANOFI-AVENTIS CANADA INC
Molecule: CALCITONIN (SALMON SYNTHETIC)
Available to quote
Health Canada record
| Active ingredient(s) | CALCITONIN (SALMON SYNTHETIC) 200 UNIT |
|---|---|
| Dosage form | Solution |
| Route | Subcutaneous; Intramuscular |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | H05BA01 CALCITONIN (SALMON SYNTHETIC) |
| Original market date | 31-Dec-1983 |
| Current status date | 13-Feb-2008 |
| Source | Health Canada DPD |
Establishment licence of the holder
sanofi-aventis Canada Inc. — licence 101470, currently licensed, last inspection rating C (2026-02-17).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing CALCITONIN (SALMON SYNTHETIC)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02383233 | CALCITONIN SALMON INJECTION USP | STERIMAX INC | Solution | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Approved |
| 02144301 | MIACALCIN INJECTION 200IU/ML | NOVARTIS PHARMACEUTICALS CANADA INC | Liquid | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Approved |
| 02246058 | APO-CALCITONIN INJECTABLE | APOTEX INC | Liquid | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Cancelled Post Market |
| 02247585 | APO-CALCITONIN NASAL SPRAY | APOTEX INC | Solution | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Cancelled Post Market |
| 02007134 | CALTINE INJ 100 UNIT/ML (1ML AMP) | FERRING INC | Liquid | CALCITONIN (SALMON SYNTHETIC) 100 UNIT | Cancelled Post Market |
| 01940376 | CALTINE INJ 100UNIT/ML (0.5ML AMP) | FERRING INC | Liquid | CALCITONIN (SALMON SYNTHETIC) 100 UNIT | Cancelled Post Market |
| 02240775 | MIACALCIN NASAL SPRAY 200 IU | NOVARTIS PHARMACEUTICALS CANADA INC | Spray | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Cancelled Post Market |
| 02311046 | PRO-CALCITONIN - 200 | PRO DOC LIMITEE | Solution | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Cancelled Post Market |
| 02261766 | SANDOZ-CALCITONIN NS | SANDOZ CANADA INCORPORATED | Liquid | CALCITONIN (SALMON SYNTHETIC) 200 UNIT | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 7976 | 2006-05-18 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 1470 | 2000-10-24 | New Drug Submission (NDS) |