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NDC 24208-0734-05 Fluorescein Sodium and Benoxinate Hydrochloride 4.4; 2.6 mg/mL; mg/mL Details
Fluorescein Sodium and Benoxinate Hydrochloride 4.4; 2.6 mg/mL; mg/mL
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 Information
| NDC | 24208-0734 |
|---|---|
| Product ID | 24208-734_bc60e95e-6fb2-4e5f-a5df-40490b2ee204 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Active Ingredient Strength | 4.4; 2.6 |
| Active Ingredient Units | mg/mL; mg/mL |
| Substance Name | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM |
| Labeler Name | Bausch & Lomb Incorporated |
| Pharmaceutical Class | Diagnostic Dye [EPC], Dyes [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA211039 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 24208-0734-05 (24208073405)
| NDC Package Code | 24208-734-05 |
|---|---|
| Billing NDC | 24208073405 |
| Package | 1 BOTTLE, GLASS in 1 CARTON (24208-734-05) / 5 mL in 1 BOTTLE, GLASS |
| Marketing Start Date | 2020-03-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |