Home
>
National Drug Code (NDC)
>
Fluorescein Sodium and Benoxinate Hydrochloride
Fluorescein Sodium and Benoxinate Hydrochloride - 24208-732-05 - (Fluorescein Sodium and Benoxinate Hydrochloride)
Drug Information of Fluorescein Sodium and Benoxinate Hydrochloride
| Product NDC: | 24208-732 |
| Proprietary Name: | Fluorescein Sodium and Benoxinate Hydrochloride |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluorescein Sodium and Benoxinate Hydrochloride
| Product NDC: | 24208-732 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19950101 |
Package Information of Fluorescein Sodium and Benoxinate Hydrochloride
| Package NDC: | 24208-732-05 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (24208-732-05) > 5 mL in 1 BOTTLE, GLASS |
NDC Information of Fluorescein Sodium and Benoxinate Hydrochloride
| NDC Code | 24208-732-05 |
| Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (24208-732-05) > 5 mL in 1 BOTTLE, GLASS |
| Product NDC | 24208-732 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19950101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM |
| Strength Number | 4; 2.5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Diagnostic Dye [EPC],Dyes [MoA] |
