Fludeoxyglucose F 18
- Product NDC
- 76167-001
- 11-digit product format
- 761670001
- Labeler code
- 76167
- Product ID
- 76167-001_a379225a-0a67-4965-8c08-87f33318dc85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUDEOXYGLUCOSE F-18
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Children's Hospital of Michigan
- Application
- ANDA204385
- Marketing category
- ANDA
- Marketing start
- 2014-11-12
- 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