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Kit for the Preparation of Technetium Tc99m Disofenin - 45567-0475-1 - (HEPATOLITE)

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Drug Information of Kit for the Preparation of Technetium Tc99m Disofenin

Product NDC: 45567-0475
Proprietary Name: Kit for the Preparation of Technetium Tc99m Disofenin
Non Proprietary Name: HEPATOLITE
Active Ingredient(s): 20    mg/10mL & nbsp;   HEPATOLITE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Kit for the Preparation of Technetium Tc99m Disofenin

Product NDC: 45567-0475
Labeler Name: Pharmalucence, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018467
Marketing Category: NDA
Start Marketing Date: 19820316

Package Information of Kit for the Preparation of Technetium Tc99m Disofenin

Package NDC: 45567-0475-1
Package Description: 5 VIAL in 1 KIT (45567-0475-1) > 10 mL in 1 VIAL

NDC Information of Kit for the Preparation of Technetium Tc99m Disofenin

NDC Code 45567-0475-1
Proprietary Name Kit for the Preparation of Technetium Tc99m Disofenin
Package Description 5 VIAL in 1 KIT (45567-0475-1) > 10 mL in 1 VIAL
Product NDC 45567-0475
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEPATOLITE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19820316
Marketing Category Name NDA
Labeler Name Pharmalucence, Inc.
Substance Name DISOFENIN
Strength Number 20
Strength Unit mg/10mL
Pharmaceutical Classes Radioactive Diagnostic Agent [EPC],Radiopharmaceutical Activity [MoA]

Complete Information of Kit for the Preparation of Technetium Tc99m Disofenin


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