NDC product
Sodium Fluoride F 18
NDC 24562-002 · Biomedical Research Foundation of Northwest Louisiana
Key facts
| Product NDC | 24562-002 |
|---|---|
| Proprietary name | Sodium Fluoride F 18 |
| Nonproprietary name | SODIUM FLUORIDE F-18 |
| Substances | SODIUM FLUORIDE F-18 |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Labeler | Biomedical Research Foundation of Northwest Louisiana |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA204351 |
| Pharmacologic classes | Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA] |
| Marketing start | Jan 22, 2015 |
| Listing certified through | Dec 31, 2027 |
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: