NDC product
Fludeoxyglucose F18
NDC 24275-0185 · UCSF Radiopharmaceutical Facility
Key facts
| Product NDC | 24275-0185 |
|---|---|
| Proprietary name | Fludeoxyglucose F18 |
| Nonproprietary name | Fludeoxyglucose F18 |
| Substances | FLUDEOXYGLUCOSE F-18 |
| Dosage form | INJECTION |
| Route | INTRAVENOUS |
| Labeler | UCSF Radiopharmaceutical Facility |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA203902 |
| Pharmacologic classes | Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA] |
| Marketing start | Dec 4, 2011 |
| Listing certified through | Dec 31, 2026 |
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: