Discontinuation report BETOPTIC S
Report ID | 170389 |
Drug Identification Number | 01908448 |
Brand name | BETOPTIC S |
Common or Proper name | BETOPTIC S 0.25% SUSP. |
Company Name | NOVARTIS PHARMACEUTICALS CANADA INC |
Market Status | MARKETED |
Active Ingredient(s) | BETAXOLOL |
Strength(s) | 0.25% |
Dosage form(s) | SUSPENSION |
Route of administration | OPHTHALMIC OPHTHALMIC |
Packaging size | 10ML |
ATC code | S01ED |
ATC description | ANTIGLAUCOMA PREPARATIONS AND MIOTICS |
Reason for discontinuation | Business reasons |
Anticipated discontinuation date | 2022-11-30 |
Actual discontinuation date | 2022-12-29 |
Remaining supply date | 2023-07-31 |
Discontinuation status | Discontinued |
Discontinuation decision reversal | No |
Information on remaining supply | |
Company comments | Betoptic S 0.25% Susp. 5mL will continue to be available. |
Health Canada comments | |
Tier 3 Status | No |
Contact Address | 700 RUE SAINT-HUBERT MONTREAL, QUEBEC CANADA H2Y 0C1 |
Company contact information | customer.relations@novartis.com |
Version History
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Version Number | Date Updated | Language | |
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v10 | 2023-01-19 | French | Compare |
v9 | 2023-01-19 | English | Compare |
v8 | 2022-09-29 | French | Compare |
v7 | 2022-09-29 | English | Compare |
v6 | 2022-09-28 | French | Compare |
v5 | 2022-09-28 | English | Compare |
v4 | 2022-09-28 | French | Compare |
v3 | 2022-09-28 | English | Compare |
v2 | 2022-09-28 | English | Compare |
v1 | 2022-09-28 | English | Compare |
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