FLURESS is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Akorn, Inc.. The primary component is Fluorescein Sodium; Benoxinate Hydrochloride.
Product ID | 17478-640_b63db481-5b90-4817-b2f9-940ba2473d0b |
NDC | 17478-640 |
Product Type | Human Prescription Drug |
Proprietary Name | FLURESS |
Generic Name | Fluorescein Sodium And Benoxinate Hydrochloride |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 1995-02-01 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Akorn, Inc. |
Substance Name | FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE |
Active Ingredient Strength | 3 mg/mL; mg/mL |
Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 1995-02-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-02-01 |
Ingredient | Strength |
---|---|
FLUORESCEIN SODIUM | 2.5 mg/mL |
SPL SET ID: | b8cd0372-88f4-4f21-8991-3fec828537ef |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
17478-640 | FLURESS | Fluorescein Sodium and Benoxinate Hydrochloride |
59390-206 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
59390-218 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
24208-732 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
24208-734 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
68682-732 | Fluorescein Sodium and Benoxinate Hydrochloride | Fluorescein Sodium and Benoxinate Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLURESS 72203731 0789323 Live/Registered |
BARNES HIND LABORATORIES 1964-10-12 |