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In-111 DTPA - 51808-125-01 - (In-111 DTPA)

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Drug Information of In-111 DTPA

Product NDC: 51808-125
Proprietary Name: In-111 DTPA
Non Proprietary Name: In-111 DTPA
Active Ingredient(s): 3.75    mCi/1.5mL & nbsp;   In-111 DTPA
Administration Route(s): INTRATHECAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of In-111 DTPA

Product NDC: 51808-125
Labeler Name: AnazaoHealth Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120619

Package Information of In-111 DTPA

Package NDC: 51808-125-01
Package Description: 1.5 mL in 1 VIAL (51808-125-01)

NDC Information of In-111 DTPA

NDC Code 51808-125-01
Proprietary Name In-111 DTPA
Package Description 1.5 mL in 1 VIAL (51808-125-01)
Product NDC 51808-125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name In-111 DTPA
Dosage Form Name SOLUTION
Route Name INTRATHECAL
Start Marketing Date 20120619
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name AnazaoHealth Corporation
Substance Name INDIUM IN-111 PENTETATE DISODIUM
Strength Number 3.75
Strength Unit mCi/1.5mL
Pharmaceutical Classes Lead Chelating Activity [MoA],Lead Chelator [EPC]

Complete Information of In-111 DTPA


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