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Fludeoxyglucose F 18
Fludeoxyglucose F 18 - 49609-101-01 - (Fludeoxyglucose F-18)
Drug Information of Fludeoxyglucose F 18
| Product NDC: | 49609-101 |
| Proprietary Name: | Fludeoxyglucose F 18 |
| Non Proprietary Name: | Fludeoxyglucose F-18 |
| Active Ingredient(s): | 300 mCi/mL & nbsp; Fludeoxyglucose F-18 |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fludeoxyglucose F 18
| Product NDC: | 49609-101 |
| Labeler Name: | IBA Molecular North America, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111208 |
Package Information of Fludeoxyglucose F 18
| Package NDC: | 49609-101-01 |
| Package Description: | 30 mL in 1 VIAL, MULTI-DOSE (49609-101-01) |
NDC Information of Fludeoxyglucose F 18
| NDC Code | 49609-101-01 |
| Proprietary Name | Fludeoxyglucose F 18 |
| Package Description | 30 mL in 1 VIAL, MULTI-DOSE (49609-101-01) |
| Product NDC | 49609-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fludeoxyglucose F-18 |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111208 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | IBA Molecular North America, Inc. |
| Substance Name | FLUDEOXYGLUCOSE F-18 |
| Strength Number | 300 |
| Strength Unit | mCi/mL |
| Pharmaceutical Classes | Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA] |
