Discontinuation report FLURESS
| Report ID | 135284 |
| Drug Identification Number | 02216728 |
| Brand name | FLURESS |
| Common or Proper name | fluorescein sodium and benoxinate hydrochloride solution |
| Company Name | AKORN INC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | FLUORESCEIN SODIUM BENOXINATE HYDROCHLORIDE |
| Strength(s) | 0.25% 0.4% |
| Dosage form(s) | SOLUTION |
| Route of administration | OPHTHALMIC |
| Packaging size | 5mL |
| ATC code | S01JA |
| ATC description | DIAGNOSTICAGENTS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2021-02-22 |
| Remaining supply date | 2014-08-31 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 1925 WEST FIELD CT LAKE FOREST, ILLINOIS UNITED STATES 60045 |
| Company contact information |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v2 | 2021-03-08 | French | Compare |
| v1 | 2021-03-08 | English | Compare |
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