NDC product
Procainamide Hydrochloride
NDC 0409-1903 · Hospira, Inc.
Key facts
| Product NDC | 0409-1903 |
|---|---|
| Proprietary name | Procainamide Hydrochloride |
| Labeler | Hospira, Inc. |
| Marketing category | ANDA |
| Application number | ANDA089070 |
| Marketing start | Aug 29, 2005 |
| Marketing end | Feb 10, 2026 |
| Listing certified through | Feb 10, 2026 |
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: