NDC product
lidocaine hydrochloride
NDC 0517-9405 · American Regent, Inc.
Key facts
| Product NDC | 0517-9405 |
|---|---|
| Proprietary name | lidocaine hydrochloride |
| Labeler | American Regent, Inc. |
| Marketing category | ANDA |
| Application number | ANDA091564 |
| Marketing start | Sep 14, 2015 |
| Marketing end | Oct 14, 2015 |
| Listing certified through | Oct 14, 2015 |
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: