FLUORESCITE is a Ophthalmic Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Fluorescein Sodium.
Product ID | 0065-0092_362ba67f-abf9-4210-a994-3814ca7bbb06 |
NDC | 0065-0092 |
Product Type | Human Prescription Drug |
Proprietary Name | FLUORESCITE |
Generic Name | Fluorescein Sodium |
Dosage Form | Injection, Solution |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 1972-09-15 |
Marketing Category | NDA / NDA |
Application Number | NDA021980 |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | FLUORESCEIN SODIUM |
Active Ingredient Strength | 100 mg/mL |
Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1972-09-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021980 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1972-09-15 |
Marketing End Date | 2013-10-31 |
Marketing Category | NDA |
Application Number | NDA021980 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1972-09-15 |
Ingredient | Strength |
---|---|
FLUORESCEIN SODIUM | 100 mg/mL |
SPL SET ID: | ebb3883c-71f6-4fd0-a7e6-0ba8e1136dd9 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
0065-0092 | FLUORESCITE | fluorescein sodium |
17478-250 | AK-FLUOR | fluorescein sodium |
17478-253 | AK-FLUOR | fluorescein sodium |
50090-4535 | AK-FLUOR | fluorescein sodium |
17238-900 | BioGlo | Fluorescein Sodium |
51801-008 | Dry Eye Test | Fluorescein Sodium |
17478-403 | FUL-GLO | Fluorescein Sodium |
17478-404 | FUL-GLO | Fluorescein Sodium |
51801-003 | GloStrips | Fluorescein Sodium |
51801-009 | GloStrips | Fluorescein Sodium |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLUORESCITE 72359790 0900633 Live/Registered |
C. F. KIRK LABORATORIES, INC. 1970-05-15 |