Fludeoxyglucose F 18
- Product NDC
- 21731-647
- 11-digit product format
- 217310647
- Labeler code
- 21731
- Product ID
- 21731-647_40c84846-12b0-1c39-b71d-f474c4ade667
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F 18
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Centre for Probe Development and Commercialization
- Application
- ANDA204525
- Marketing category
- ANDA
- Marketing start
- 2014-10-29
- 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