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 Fluorescein Sodium; Benoxinate Hydrochloride.
| Product ID | 24208-734_1797c5ef-66c4-4cf8-b62d-b484242be2ee |
| NDC | 24208-734 |
| 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 | 2020-03-20 |
| Marketing Category | NDA / NDA |
| Application Number | NDA211039 |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/mL; mg/mL |
| Pharm Classes | Diagnostic Dye [EPC],Dyes [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2020-03-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA211039 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-03-20 |
| Ingredient | Strength |
|---|---|
| FLUORESCEIN SODIUM | 2.6 mg/mL |
| 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 |