AK-FLUOR is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Akorn. The primary component is Fluorescein Sodium.
Product ID | 17478-253_2e04a625-512e-4c19-a546-f164c363ad19 |
NDC | 17478-253 |
Product Type | Human Prescription Drug |
Proprietary Name | AK-FLUOR |
Generic Name | Fluorescein Sodium |
Dosage Form | Injection |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2008-10-01 |
Marketing Category | NDA / NDA |
Application Number | NDA022186 |
Labeler Name | Akorn |
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 | 2008-10-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022186 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2008-10-01 |
Ingredient | Strength |
---|---|
FLUORESCEIN SODIUM | 100 mg/mL |
SPL SET ID: | a1823be3-a739-48bc-a3ea-ceb7cc5105ce |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
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 |
0065-0092 | FLUORESCITE | 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 |
---|---|
AK-FLUOR 73652686 1464246 Live/Registered |
AKORN, INC. 1987-04-02 |