NDC product
Fluorescein Sodium and Benoxinate Hydrochloride
NDC 24208-734 · Bausch & Lomb Incorporated
Key facts
| Product NDC | 24208-734 |
|---|---|
| Proprietary name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Nonproprietary name | Fluorescein Sodium and Benoxinate Hydrochloride |
| Substances | FLUORESCEIN SODIUM, BENOXINATE HYDROCHLORIDE |
| Dosage form | SOLUTION/ DROPS |
| Route | OPHTHALMIC |
| Labeler | Bausch & Lomb Incorporated |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Application number | NDA211039 |
| Pharmacologic classes | Diagnostic Dye [EPC], Dyes [MoA] |
| Marketing start | Mar 20, 2020 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: