NDC product
Fosphenytoin Sodium
NDC 0703-7101 · Teva Parenteral Medicines, Inc.
Key facts
| Product NDC | 0703-7101 |
|---|---|
| Proprietary name | Fosphenytoin Sodium |
| Labeler | Teva Parenteral Medicines, Inc. |
| Marketing category | ANDA |
| Application number | ANDA076886 |
| Marketing start | Sep 14, 2007 |
| Marketing end | Aug 31, 2011 |
| Listing certified through | Aug 31, 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: