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Fludeoxyglucose F-18 - 16129-001-10 - (Fludeoxyglucose F-18)

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Drug Information of Fludeoxyglucose F-18

Product NDC: 16129-001
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: 16129-001
Labeler Name: Shertech Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20060329

Package Information of Fludeoxyglucose F-18

Package NDC: 16129-001-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (16129-001-10)

NDC Information of Fludeoxyglucose F-18

NDC Code 16129-001-10
Proprietary Name Fludeoxyglucose F-18
Package Description 10 mL in 1 VIAL, MULTI-DOSE (16129-001-10)
Product NDC 16129-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fludeoxyglucose F-18
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20060329
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Shertech Laboratories, LLC
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 F-18


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