Fludeoxyglucose F 18
- Product NDC
- 81986-001
- 11-digit product format
- 819860001
- Labeler code
- 81986
- Product ID
- 81986-001_82333885-28e4-4f1a-809b-c6c9e625d424
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludeoxyglucose F 18
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Pharmalogic Puerto Rico, Inc.
- Application
- ANDA203664
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- FLUDEOXYGLUCOSE F-18
- Active strength
- 200 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 |
|---|
| 81986-001-30 | 81986000130 | 25 mL in 1 VIAL, MULTI-DOSE (81986-001-30) | 25 ml | 2021-06-01 | 0000-00-00 | No | No | Current |