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
Click on "Compare" below to view the full report history and compare to other versions.
Version Number | Date Updated | Language | |
---|---|---|---|
v6 | 2019-04-09 | French | Compare |
v5 | 2019-04-09 | English | Compare |
v4 | 2019-02-22 | French | Compare |
v3 | 2019-02-22 | English | Compare |
v2 | 2019-01-03 | French | Compare |
v1 | 2019-01-03 | English | Compare |
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