NDC product
Sodium Fluoride F 18
NDC 13108-211 · NukeMed, Inc. dba SpectronRx
Key facts
| Product NDC | 13108-211 |
|---|---|
| Proprietary name | Sodium Fluoride F 18 |
| Labeler | NukeMed, Inc. dba SpectronRx |
| Marketing category | ANDA |
| Application number | ANDA203912 |
| Marketing start | Apr 24, 2015 |
| Marketing end | Aug 17, 2020 |
| Listing certified through | Aug 17, 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: