Sodium Fluoride F 18
- Product NDC
- 73410-002
- 11-digit product format
- 734100002
- Labeler code
- 73410
- Product ID
- 73410-002_35999220-43ed-4123-ab28-4b249ab187f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Fluoride F 18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Decatur Memorial Hospital
- Application
- ANDA204464
- Marketing category
- ANDA
- Marketing start
- 2019-11-06
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE F-18
- Active strength
- 10 mCi/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 73410-002-01 | 73410000201 | 30 mL in 1 VIAL, MULTI-DOSE (73410-002-01) | 30 ml | 2019-11-06 | 0000-00-00 | No | No | Current |