Discontinuation report GD-VENLAFAXINE XR
| Report ID | 45710 | 
| Drug Identification Number | 02360039 | 
| Brand name | GD-VENLAFAXINE XR | 
| Common or Proper name | VENLAFAXINE | 
| Company Name | GENMED A DIVISION OF PFIZER CANADA ULC | 
| Market Status | CANCELLED POST MARKET | 
| Active Ingredient(s) | VENLAFAXINE | 
| Strength(s) | 75MG | 
| Dosage form(s) | CAPSULE (EXTENDED RELEASE) | 
| Route of administration | ORAL | 
| Packaging size | 90's | 
| ATC code | N06AX | 
| ATC description | ANTIDEPRESSANTS | 
| Reason for discontinuation | Business reasons | 
| Anticipated discontinuation date | |
| Actual discontinuation date | 2018-07-12 | 
| Remaining supply date | 2018-07-30 | 
| Discontinuation status | Discontinued | 
| Discontinuation decision reversal | No | 
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No | 
| Contact Address | 17300 TRANS CANADA HIGHWAY  KIRKLAND, QUEBEC CANADA H9J 2M5  | 
				
| Company contact information | Customer Service / service à la clientèle : 1-800-387-4974 Email / courriel: [email protected] | 
Version History
Click on "Compare" below to view the full report history and compare to other versions.
| Version Number | Date Updated | Language | |
|---|---|---|---|
| v4 | 2018-07-13 | French | Compare | 
| v3 | 2018-07-13 | English | Compare | 
| v2 | 2018-04-13 | French | Compare | 
| v1 | 2018-04-13 | English | Compare | 
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