NDC product
Naloxone Hydrochloride
NDC 0548-3369 · Amphastar Pharmaceuticals, Inc.
Key facts
| Product NDC | 0548-3369 |
|---|---|
| Proprietary name | Naloxone Hydrochloride |
| Labeler | Amphastar Pharmaceuticals, Inc. |
| Marketing category | ANDA |
| Application number | ANDA072076 |
| Marketing start | Jun 1, 2001 |
| Marketing end | Jan 10, 2013 |
| Listing certified through | Jan 10, 2013 |
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: