Product NDC: | 17478-404 |
Proprietary Name: | FUL-GLO |
Non Proprietary Name: | Fluorescein Sodium |
Active Ingredient(s): | 1 mg/1 & nbsp; Fluorescein Sodium |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | STRIP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-404 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20040601 |
Package NDC: | 17478-404-01 |
Package Description: | 100 APPLICATOR in 1 CARTON (17478-404-01) > 1 STRIP in 1 APPLICATOR |
NDC Code | 17478-404-01 |
Proprietary Name | FUL-GLO |
Package Description | 100 APPLICATOR in 1 CARTON (17478-404-01) > 1 STRIP in 1 APPLICATOR |
Product NDC | 17478-404 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluorescein Sodium |
Dosage Form Name | STRIP |
Route Name | OPHTHALMIC |
Start Marketing Date | 20040601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Akorn, Inc. |
Substance Name | D&C YELLOW NO. 8 |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |