NDC product
Vancomycin Hydrochloride
NDC 45932-0032 · Xellia Pharmaceuticals ApS
Key facts
| Product NDC | 45932-0032 |
|---|---|
| Proprietary name | Vancomycin Hydrochloride |
| Labeler | Xellia Pharmaceuticals ApS |
| Marketing category | ANDA |
| Application number | ANDA206243 |
| Marketing start | Feb 10, 2015 |
| Listing certified through | Dec 31, 2019 |
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: