Discontinuation report LOTENSIN 20MG
| Report ID | 23762 |
| Drug Identification Number | 00885851 |
| Brand name | LOTENSIN 20MG |
| Common or Proper name | LOTENSIN 20MG 2 X 14 |
| Company Name | NOVARTIS PHARMACEUTICALS CANADA INC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | BENAZEPRIL HYDROCHLORIDE |
| Strength(s) | 20MG |
| Dosage form(s) | TABLET |
| Route of administration | ORAL |
|
Packaging sizes (GTIN)
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(See additional packaging sizes) |
| Additional packaging sizes | 2 X 14 |
| ATC code | C09AA |
| ATC description | ACE INHIBITORS, PLAIN |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2018-03-30 |
| Actual discontinuation date | 2018-08-28 |
| Remaining supply date | 2018-03-30 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | Lot expiring Sept 2018 |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 700 RUE SAINT-HUBERT MONTREAL, QUEBEC CANADA H2Y 0C1 |
| Company contact information | [email protected] |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v7 | 2018-08-29 | English | Compare |
| v6 | 2018-08-28 | French | Compare |
| v5 | 2018-08-28 | English | Compare |
| v4 | 2018-08-28 | French | Compare |
| v3 | 2018-08-28 | English | Compare |
| v2 | 2017-09-27 | French | Compare |
| v1 | 2017-09-27 | English | Compare |
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