NDC product
PREDNISOLONE SODIUM PHOSPHATE
NDC 13925-501 · Seton Pharmaceuticals
Key facts
| Product NDC | 13925-501 |
|---|---|
| Proprietary name | PREDNISOLONE SODIUM PHOSPHATE |
| Labeler | Seton Pharmaceuticals |
| Marketing category | ANDA |
| Application number | ANDA075183 |
| Marketing start | Mar 26, 2003 |
| Marketing end | Jul 21, 2015 |
| Listing certified through | Jul 21, 2015 |
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: