NDC product
Amlodipine Besylate
NDC 0093-0083 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-0083 |
|---|---|
| Proprietary name | Amlodipine Besylate |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Marketing category | ANDA |
| Application number | ANDA076846 |
| Marketing start | Jul 10, 2007 |
| Marketing end | Jul 19, 2017 |
| Listing certified through | Jul 19, 2017 |
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: