NDC product
DAUNORUBICIN HYDROCHLORIDE
NDC 0024-5858 · Sanofi-Aventis U.S. LLC
Key facts
| Product NDC | 0024-5858 |
|---|---|
| Proprietary name | DAUNORUBICIN HYDROCHLORIDE |
| Labeler | Sanofi-Aventis U.S. LLC |
| Marketing category | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
| Marketing start | Jun 23, 2014 |
| Marketing end | Nov 11, 2014 |
| Listing certified through | Nov 11, 2014 |
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: