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Fludeoxyglucose F-18 - 52768-001-50 - (Fludeoxyglucose F-18)

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Drug Information of Fludeoxyglucose F-18

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)

Labeler Information of Fludeoxyglucose F-18

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 Information of Fludeoxyglucose F-18

Package NDC: 52768-001-50
Package Description: 50 mL in 1 VIAL (52768-001-50)

NDC Information of Fludeoxyglucose F-18

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]

Complete Information of Fludeoxyglucose F-18


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