Discontinuation report RANITIDINE
Report ID | 76211 |
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 | 60 |
ATC code | A02BA |
ATC description | DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD) |
Reason for discontinuation | Business reasons |
Anticipated discontinuation date | 2019-05-24 |
Actual discontinuation date | 2019-05-29 |
Remaining supply date | 2019-08-01 |
Discontinuation status | Discontinued |
Discontinuation decision reversal | No |
Information on remaining supply | |
Company comments | Other pack sizes available |
Health Canada comments | |
Tier 3 Status | No |
Contact Address | 4705 DOBRIN STREET SAINT-LAURENT, QUEBEC CANADA H4R 2P7 |
Company contact information |
Version History
Click on "Compare" below to view the full report history and compare to other versions.
Version Number | Date Updated | Language | |
---|---|---|---|
v12 | 2019-05-31 | French | Compare |
v11 | 2019-05-31 | English | Compare |
v10 | 2019-05-17 | French | Compare |
v9 | 2019-05-17 | English | Compare |
v8 | 2019-05-06 | French | Compare |
v7 | 2019-05-06 | English | Compare |
v6 | 2019-04-22 | French | Compare |
v5 | 2019-04-22 | English | Compare |
v4 | 2019-04-15 | French | Compare |
v3 | 2019-04-15 | English | Compare |
v2 | 2019-02-18 | French | Compare |
v1 | 2019-02-18 | English | Compare |
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