Discontinuation report RANITIDINE
| Report ID | 70956 |
| Drug Identification Number | 02385953 |
| Brand name | RANITIDINE |
| Common or Proper name | RANITIDINE |
| Company Name | SIVEM PHARMACEUTICALS ULC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | RANITIDINE |
| Strength(s) | 150MG |
| Dosage form(s) | TABLET |
| Route of administration | ORAL |
| Packaging size | 100 |
| ATC code | A02BA |
| ATC description | DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD) |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2019-04-01 |
| Actual discontinuation date | 2019-04-02 |
| Remaining supply date | 2019-04-30 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | Other pack size available |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 4705 DOBRIN STREET SAINT-LAURENT, QUEBEC CANADA H4R 2P7 |
| Company contact information |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v1 | 2019-01-03 | English | Compare |
| v2 | 2019-01-03 | French | Compare |
| v3 | 2019-02-22 | English | Compare |
| v4 | 2019-02-22 | French | Compare |
| v5 | 2019-04-09 | English | Compare |
| v6 | 2019-04-09 | French | Compare |
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