Product NDC: | 17478-250 |
Proprietary Name: | AK-FLUOR |
Non Proprietary Name: | fluorescein sodium |
Active Ingredient(s): | 250 mg/mL & nbsp; fluorescein sodium |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-250 |
Labeler Name: | Akorn |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022186 |
Marketing Category: | NDA |
Start Marketing Date: | 20081001 |
Package NDC: | 17478-250-20 |
Package Description: | 12 VIAL, SINGLE-DOSE in 1 PACKAGE (17478-250-20) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 17478-250-20 |
Proprietary Name | AK-FLUOR |
Package Description | 12 VIAL, SINGLE-DOSE in 1 PACKAGE (17478-250-20) > 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 17478-250 |
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 | 250 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |