Fludeoxyglucose F18
- Product NDC
- 51760-001
- 11-digit product format
- 517600001
- Labeler code
- 51760
- Product ID
- 51760-001_7654ceab-cbcd-4e5f-848d-35f813dc0ddf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Essential Isotopes LLC
- Application
- ANDA203946
- Marketing category
- ANDA
- Marketing start
- 2005-08-19
- Marketing end
- 0000-00-00
- Substance
- FLUDEOXYGLUCOSE F-18
- Active strength
- 300 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 |
|---|
| 51760-001-30 | 51760000130 | 30 mL in 1 VIAL, GLASS (51760-001-30) | 30 ml | 2005-08-19 | 0000-00-00 | No | No | Current |