FORTEKOR FLAVOR TABS DIN 02305232
Health Canada record
| Active ingredient(s) | BENAZEPRIL HYDROCHLORIDE 2.5 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Veterinary |
| ATC | |
| Original market date | 05-Aug-2008 |
| Current status date | 16-Sep-2016 |
| Source | Health Canada DPD |
Establishment licence of the holder
Elanco Canada Limited — licence 102236, currently licensed, last inspection rating C (2022-08-03).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing BENAZEPRIL HYDROCHLORIDE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02290340 | BENAZEPRIL | AA PHARMA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 10 MG | Marketed |
| 02273918 | BENAZEPRIL | AA PHARMA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 20 MG | Marketed |
| 02290332 | BENAZEPRIL | AA PHARMA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 5 MG | Marketed |
| 02542099 | CARDALIS | CEVA ANIMAL HEALTH INC | Tablet (Chewable) | BENAZEPRIL HYDROCHLORIDE 10 MG; SPIRONOLACTONE 80 MG | Approved |
| 02542102 | CARDALIS | CEVA ANIMAL HEALTH INC | Tablet (Chewable) | BENAZEPRIL HYDROCHLORIDE 2.5 MG; SPIRONOLACTONE 20 MG | Marketed |
| 02542080 | CARDALIS | CEVA ANIMAL HEALTH INC | Tablet (Chewable) | BENAZEPRIL HYDROCHLORIDE 5 MG; SPIRONOLACTONE 40 MG | Marketed |
| 02220555 | FORTEKOR FLAVOR TABS | ELANCO CANADA LIMITED | Tablet | BENAZEPRIL HYDROCHLORIDE 20 MG | Marketed |
| 02220563 | FORTEKOR FLAVOR TABS | ELANCO CANADA LIMITED | Tablet | BENAZEPRIL HYDROCHLORIDE 5 MG | Marketed |
| 00885843 | LOTENSIN 10MG | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 10 MG | Cancelled Post Market |
| 00885851 | LOTENSIN 20MG | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 20 MG | Cancelled Post Market |
| 00885835 | LOTENSIN 5MG | NOVARTIS PHARMACEUTICALS CANADA INC | Tablet | BENAZEPRIL HYDROCHLORIDE 5 MG | Cancelled Post Market |
| 02231551 | PMS-BENAZEPRIL | PHARMASCIENCE INC | Tablet | BENAZEPRIL HYDROCHLORIDE 20 MG | Cancelled Pre Market |
| 02231550 | PMS-BENAZEPRIL | PHARMASCIENCE INC | Tablet | BENAZEPRIL HYDROCHLORIDE 10 MG | Cancelled Pre Market |
| 02231548 | PMS-BENAZEPRIL | PHARMASCIENCE INC | Tablet | BENAZEPRIL HYDROCHLORIDE 5 MG | Cancelled Pre Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 20734 | 2018-04-12 | Supplement to a New Drug Submission (SNDS) | New Manufacturer and testing site. |
| 23280 | 2016-09-16 | New Drug Submission (NDS) | MERGER - BUYOUT |
| 9335 | 2008-01-30 | New Drug Submission (NDS) |
International API supply for BENAZEPRIL HYDROCHLORIDE
7 valid EDQM Certificates of Suitability from 7 holders. 14 active FDA Drug Master Files.
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