NDC product
Timolol Maleate
NDC 24208-818 · Bausch & Lomb Incorporated
Key facts
| Product NDC | 24208-818 |
|---|---|
| Proprietary name | Timolol Maleate |
| Labeler | Bausch & Lomb Incorporated |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA020330 |
| Marketing start | Feb 14, 2018 |
| Marketing end | Dec 17, 2025 |
| Listing certified through | Dec 17, 2025 |
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: