Fludeoxyglucose F18
- Product NDC
- 69815-754
- 11-digit product format
- 698150754
- Labeler code
- 69815
- Product ID
- 69815-754_db117a28-f553-4c60-b531-79a3498b62f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Memorial Sloan Kettering Cancer Center
- Application
- ANDA208679
- Marketing category
- ANDA
- Marketing start
- 2015-04-08
- 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
- 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 |
|---|
| 69815-754-50 | 69815075450 | 50 mL in 1 VIAL, GLASS (69815-754-50) | 50 ml | 2016-12-16 | 0000-00-00 | No | No | Current |