NDC product
Helixate FS
NDC 0053-8132 · CSL Behring LLC
Key facts
| Product NDC | 0053-8132 |
|---|---|
| Proprietary name | Helixate FS |
| Labeler | CSL Behring LLC |
| Marketing category | BLA |
| Application number | BLA103332 |
| Marketing start | Aug 18, 2000 |
| Marketing end | Jul 10, 2020 |
| Listing certified through | Jul 10, 2020 |
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: