NTP-TELMISARTAN HCTZ DIN 02388758
Status: Cancelled Pre Market
Holder: TEVA CANADA LIMITED
Health Canada record
| Active ingredient(s) | TELMISARTAN (TELMISARTAN SODIUM) 80.0 MG; HYDROCHLOROTHIAZIDE 12.5 MG |
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| Dosage form | Tablet |
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| Route | Oral |
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| Schedule | PRESCRIPTION |
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| Class | Human |
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| ATC | C09DA07 TELMISARTAN AND DIURETICS |
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| Original market date | |
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| Current status date | 13-Jun-2017 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing TELMISARTAN (TELMISARTAN SODIUM)
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02330288 | TEVA-TELMISARTAN HCTZ | TEVA CANADA LIMITED | Tablet | TELMISARTAN (TELMISARTAN SODIUM) 80 MG; HYDROCHLOROTHIAZIDE 12.5 MG | Marketed |
| 02379252 | TEVA-TELMISARTAN HCTZ | TEVA CANADA LIMITED | Tablet | TELMISARTAN (TELMISARTAN SODIUM) 80.0 MG; HYDROCHLOROTHIAZIDE 25.0 MG | Marketed |
| 02388782 | NTP-TELMISARTAN HCTZ | TEVA CANADA LIMITED | Tablet | TELMISARTAN (TELMISARTAN SODIUM) 80.0 MG; HYDROCHLOROTHIAZIDE 25.0 MG | Cancelled Pre Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 14781 | 2013-10-04 | Abbreviated New Drug Submission (ANDS) | MERGER/BUYOUT |
| 13478 | 2012-07-12 | Abbreviated New Drug Submission (ANDS) | New manufacturer and product name |
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