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Tetrofosmin - 51808-223-02 - (Tetrofosmin)

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Drug Information of Tetrofosmin

Product NDC: 51808-223
Proprietary Name: Tetrofosmin
Non Proprietary Name: Tetrofosmin
Active Ingredient(s): .35    mg/1 & nbsp;   Tetrofosmin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tetrofosmin

Product NDC: 51808-223
Labeler Name: AnazaoHealth Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120523

Package Information of Tetrofosmin

Package NDC: 51808-223-02
Package Description: 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-223-02)

NDC Information of Tetrofosmin

NDC Code 51808-223-02
Proprietary Name Tetrofosmin
Package Description 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-223-02)
Product NDC 51808-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tetrofosmin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120523
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name AnazaoHealth Corporation
Substance Name TETROFOSMIN
Strength Number .35
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Tetrofosmin


General Information