Discontinuation report M-RANITIDINE
Report ID | 124425 |
Drug Identification Number | 02473542 |
Brand name | M-RANITIDINE |
Common or Proper name | Ranitidine |
Company Name | MANTRA PHARMA INC |
Market Status | CANCELLED POST MARKET |
Active Ingredient(s) | RANITIDINE |
Strength(s) | 300MG |
Dosage form(s) | TABLET |
Route of administration | ORAL 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 | |
Actual discontinuation date | 2020-09-14 |
Remaining supply date | 2020-09-14 |
Discontinuation status | Discontinued |
Discontinuation decision reversal | No |
Information on remaining supply | |
Company comments | |
Health Canada comments | |
Tier 3 Status | No |
Contact Address | 1000 RUE DU LUX SUITE 201 BROSSARD, QUEBEC CANADA J4Y 0E3 |
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 | |
---|---|---|---|
v1 | 2020-09-17 | English | Compare |
v2 | 2020-09-17 | English | Compare |
v3 | 2020-09-17 | French | Compare |
v4 | 2020-09-17 | English | Compare |
v5 | 2020-09-17 | English | Compare |
v6 | 2020-09-17 | English | Compare |
v7 | 2020-09-17 | English | Compare |
v8 | 2020-09-17 | French | Compare |
v9 | 2020-09-17 | English | Compare |
v10 | 2020-09-17 | French | Compare |
v11 | 2020-09-17 | English | Compare |
v12 | 2020-09-17 | French | Compare |
Showing 1 to 12 of 12