Sodium Fluoride F 18
- Product NDC
- 24445-623
- 11-digit product format
- 244450623
- Labeler code
- 24445
- Product ID
- 24445-623_71e3ff00-afa8-437f-8518-43526e0fb748
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM FLUORIDE F 18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- NCM USA Bronx LLC
- Application
- ANDA204513
- Marketing category
- ANDA
- Marketing start
- 2014-10-28
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE F-18
- Active strength
- 200 mCi/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24445-623-30 | 24445062330 | 30 mL in 1 VIAL, GLASS (24445-623-30) | 30 ml | 2014-10-28 | 0000-00-00 | No | No | Current |