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Fludeoxyglucose - 24562-001-30 - (Fludeoxyglucose F-18)

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Drug Information of Fludeoxyglucose

Product NDC: 24562-001
Proprietary Name: Fludeoxyglucose
Non Proprietary Name: Fludeoxyglucose F-18
Active Ingredient(s): 300    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

Product NDC: 24562-001
Labeler Name: Biomedical Research Foundation of Northwest Louisiana
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20111212

Package Information of Fludeoxyglucose

Package NDC: 24562-001-30
Package Description: 30 mL in 1 VIAL, GLASS (24562-001-30)

NDC Information of Fludeoxyglucose

NDC Code 24562-001-30
Proprietary Name Fludeoxyglucose
Package Description 30 mL in 1 VIAL, GLASS (24562-001-30)
Product NDC 24562-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludeoxyglucose F-18
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111212
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Biomedical Research Foundation of Northwest Louisiana
Substance Name FLUDEOXYGLUCOSE F-18
Strength Number 300
Strength Unit mCi/mL
Pharmaceutical Classes Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of Fludeoxyglucose


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