NDC product
Escitalopram Oxalate
NDC 17856-0551 · ATLANTIC BIOLOGICALS CORP
Key facts
| Product NDC | 17856-0551 |
|---|---|
| Proprietary name | Escitalopram Oxalate |
| Labeler | ATLANTIC BIOLOGICALS CORP |
| Marketing category | ANDA |
| Application number | ANDA090477 |
| Marketing start | May 30, 2013 |
| Marketing end | May 1, 2022 |
| Listing certified through | May 1, 2022 |
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: