NDC product
URISPAS
NDC 17314-9220 · ALZA Corporation
Key facts
| Product NDC | 17314-9220 |
|---|---|
| Proprietary name | URISPAS |
| Labeler | ALZA Corporation |
| Marketing category | NDA |
| Application number | NDA016769 |
| Marketing start | Jan 15, 1970 |
| Marketing end | Mar 30, 2009 |
| Listing certified through | Mar 30, 2009 |
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: