NDC product
atomoxetine
NDC 68382-217 · Zydus Pharmaceuticals USA Inc.
Key facts
| Product NDC | 68382-217 |
|---|---|
| Proprietary name | atomoxetine |
| Labeler | Zydus Pharmaceuticals USA Inc. |
| Marketing category | ANDA |
| Application number | ANDA079017 |
| Marketing start | Jun 12, 2017 |
| Marketing end | Mar 21, 2025 |
| Listing certified through | Mar 21, 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: