AK-FLUOR is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Fluorescein Sodium.
| Product ID | 50090-4535_45eb1cc9-5d31-4846-93ef-e39ecf7a09d6 |
| NDC | 50090-4535 |
| 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 | A-S Medication Solutions |
| Substance Name | FLUORESCEIN SODIUM |
| Active Ingredient Strength | 100 mg/mL |
| Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-09-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA022186 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-09-18 |
| Ingredient | Strength |
|---|---|
| FLUORESCEIN SODIUM | 100 mg/mL |
| SPL SET ID: | e18fb095-d580-433c-88c5-f234f509a00f |
| 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 |