Drug · DIN 02216728
FLURESS
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since March 1, 2021; first marketed December 18, 1996.
- Drug Identification Number (DIN)
- 02216728
- Company (DIN owner)
- Akorn IncLake Forest, Illinois, United States
- Schedule
- Ethical
- Dosage form
- Solution
- Route
- Ophthalmic
- Therapeutic class (ATC)
- Fluorescein, combinations S01JA51
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| FLUORESCEIN SODIUM | 0.25 % | |
| BENOXINATE HYDROCHLORIDE | 0.4 % |