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Sodium FluorideF 18 - 76167-002-30 - (SODIUM FLUORIDE F-18)

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Drug Information of Sodium FluorideF 18

Product NDC: 76167-002
Proprietary Name: Sodium FluorideF 18
Non Proprietary Name: SODIUM FLUORIDE F-18
Active Ingredient(s): 200    mg/mL & nbsp;   SODIUM FLUORIDE F-18
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium FluorideF 18

Product NDC: 76167-002
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 Sodium FluorideF 18

Package NDC: 76167-002-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (76167-002-30)

NDC Information of Sodium FluorideF 18

NDC Code 76167-002-30
Proprietary Name Sodium FluorideF 18
Package Description 30 mL in 1 VIAL, MULTI-DOSE (76167-002-30)
Product NDC 76167-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM FLUORIDE F-18
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 SODIUM FLUORIDE F-18
Strength Number 200
Strength Unit mg/mL
Pharmaceutical Classes Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of Sodium FluorideF 18


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