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FludeoxyglucoseF18 - 76167-001-30 - (Fludeoxyglucose F18)

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Drug Information of FludeoxyglucoseF18

Product NDC: 76167-001
Proprietary Name: FludeoxyglucoseF18
Non Proprietary Name: Fludeoxyglucose F18
Active Ingredient(s): 300    mCi/mL & nbsp;   Fludeoxyglucose F18
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of FludeoxyglucoseF18

Product NDC: 76167-001
Labeler Name: Children's Hospital of Michigan
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120612

Package Information of FludeoxyglucoseF18

Package NDC: 76167-001-30
Package Description: 30 mL in 1 VIAL, GLASS (76167-001-30)

NDC Information of FludeoxyglucoseF18

NDC Code 76167-001-30
Proprietary Name FludeoxyglucoseF18
Package Description 30 mL in 1 VIAL, GLASS (76167-001-30)
Product NDC 76167-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludeoxyglucose F18
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20120612
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Children's Hospital of Michigan
Substance Name FLUDEOXYGLUCOSE F-18
Strength Number 300
Strength Unit mCi/mL
Pharmaceutical Classes Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of FludeoxyglucoseF18


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