Fludeoxyglucose F 18
- Product NDC
- 13108-111
- 11-digit product format
- 131080111
- Labeler code
- 13108
- Product ID
- 13108-111_b7c4216a-2f7a-4c16-e053-2a95a90a6118
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F 18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- NukeMed, Inc. dba SpectronRx
- Application
- ANDA203911
- Marketing category
- ANDA
- Marketing start
- 2015-04-24
- Marketing end
- 0000-00-00
- Substance
- FLUDEOXYGLUCOSE F-18
- Active strength
- 500 mCi/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 13108-111-10 | 13108011110 | 1 mL in 1 VIAL, GLASS (13108-111-10) | 1 ml | 2015-04-24 | 0000-00-00 | No | No | Current |
| 13108-111-25 | 13108011125 | 1 mL in 1 VIAL, GLASS (13108-111-25) | 1 ml | 2015-04-24 | 0000-00-00 | No | No | Current |
| 13108-111-30 | 13108011130 | 1 mL in 1 VIAL, GLASS (13108-111-30) | 1 ml | 2015-04-24 | 0000-00-00 | No | No | Current |
| 13108-111-50 | 13108011150 | 1 mL in 1 VIAL, GLASS (13108-111-50) | 1 ml | 2015-04-24 | 0000-00-00 | No | No | Current |