| Product NDC: | 17478-253 |
| Proprietary Name: | AK-FLUOR |
| Non Proprietary Name: | fluorescein sodium |
| Active Ingredient(s): | 100 mg/mL & nbsp; fluorescein sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17478-253 |
| Labeler Name: | Akorn |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022186 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081001 |
| Package NDC: | 17478-253-10 |
| Package Description: | 12 VIAL, SINGLE-DOSE in 1 PACKAGE (17478-253-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 17478-253-10 |
| Proprietary Name | AK-FLUOR |
| Package Description | 12 VIAL, SINGLE-DOSE in 1 PACKAGE (17478-253-10) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 17478-253 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluorescein sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20081001 |
| Marketing Category Name | NDA |
| Labeler Name | Akorn |
| Substance Name | FLUORESCEIN SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |