| Product NDC: | 52768-001 |
| Proprietary Name: | Fludeoxyglucose F-18 |
| Non Proprietary Name: | Fludeoxyglucose F-18 |
| Active Ingredient(s): | 500 mCi/mL & nbsp; Fludeoxyglucose F-18 |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52768-001 |
| Labeler Name: | Precision Nuclear LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101010 |
| Package NDC: | 52768-001-50 |
| Package Description: | 50 mL in 1 VIAL (52768-001-50) |
| NDC Code | 52768-001-50 |
| Proprietary Name | Fludeoxyglucose F-18 |
| Package Description | 50 mL in 1 VIAL (52768-001-50) |
| Product NDC | 52768-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fludeoxyglucose F-18 |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20101010 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Precision Nuclear LLC |
| Substance Name | FLUDEOXYGLUCOSE F-18 |
| Strength Number | 500 |
| Strength Unit | mCi/mL |
| Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |