Fludeoxyglucose F 18
- Product NDC
- 76394-3811
- 11-digit product format
- 763943811
- Labeler code
- 76394
- Product ID
- 76394-3811_eec89f5e-783b-d6ac-e053-2a95a90abdc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F 18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- University of California, Los Angeles
- Application
- ANDA203811
- Marketing category
- ANDA
- Marketing start
- 2013-06-27
- Marketing end
- 0000-00-00
- Substance
- FLUDEOXYGLUCOSE F-18
- Active strength
- 40 mCi/mL
- Pharmacologic classes
- Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 76394-3811-3 | 76394381103 | 30 mL in 1 VIAL, MULTI-DOSE (76394-3811-3) | 30 ml | 2013-06-27 | 0000-00-00 | No | No | Current |