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 | |
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v2 | 2021-03-08 | French | Compare |
v1 | 2021-03-08 | English | Compare |
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