Fluorescein Sodium and Benoxinate Hydrochloride is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Benoxinate Hydrochloride; Fluorescein Sodium.
Product ID | 24208-732_71938df7-eb38-4a21-9267-ea4b355b8c1e |
NDC | 24208-732 |
Product Type | Human Prescription Drug |
Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
Generic Name | Fluorescein Sodium And Benoxinate Hydrochloride |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 1995-01-01 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM |
Active Ingredient Strength | 4 mg/mL; mg/mL |
Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1995-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1995-01-01 |
Ingredient | Strength |
---|---|
BENOXINATE HYDROCHLORIDE | 4 mg/mL |
SPL SET ID: | 1c5a620f-7083-4fee-99e2-c9380541c368 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
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 |
59390-206 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
59390-218 | ALTAFLUOR | Fluorescein Sodium and Benoxinate Hydrochloride |
17478-640 | FLURESS | Fluorescein Sodium and Benoxinate Hydrochloride |