NDC product
Citalopram Hydrobromide
NDC 24236-727 · REMEDYREPACK INC.
Key facts
| Product NDC | 24236-727 |
|---|---|
| Proprietary name | Citalopram Hydrobromide |
| Labeler | REMEDYREPACK INC. |
| Marketing category | ANDA |
| Application number | ANDA077031 |
| Marketing start | Jun 25, 2008 |
| Marketing end | Dec 20, 2011 |
| Listing certified through | Dec 20, 2011 |
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: