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FLURESS
FLURESS - 17478-640-10 - (Fluorescein Sodium and Benoxinate Hydrochloride)
Drug Information of FLURESS
| Product NDC: | 17478-640 |
| Proprietary Name: | FLURESS |
| Non Proprietary Name: | Fluorescein Sodium and Benoxinate Hydrochloride |
| Active Ingredient(s): | 4; 2.5 mg/mL; mg/mL & nbsp; Fluorescein Sodium and Benoxinate Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLURESS
| Product NDC: | 17478-640 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19950201 |
Package Information of FLURESS
| Package NDC: | 17478-640-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-640-10) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of FLURESS
| NDC Code | 17478-640-10 |
| Proprietary Name | FLURESS |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-640-10) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-640 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19950201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Akorn, Inc. |
| Substance Name | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM |
| Strength Number | 4; 2.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |
