TechneLite - 11994-090-06 - (Molybdenum Mo-99)

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Drug Information of TechneLite

Product NDC: 11994-090
Proprietary Name: TechneLite
Non Proprietary Name: Molybdenum Mo-99
Active Ingredient(s): 250    mCi/mL & nbsp;   Molybdenum Mo-99
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of TechneLite

Product NDC: 11994-090
Labeler Name: Lantheus Medical Imaging, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017771
Marketing Category: NDA
Start Marketing Date: 19751101

Package Information of TechneLite

Package NDC: 11994-090-06
Package Description: 1 VIAL in 1 CARTON (11994-090-06) > 24 mL in 1 VIAL

NDC Information of TechneLite

NDC Code 11994-090-06
Proprietary Name TechneLite
Package Description 1 VIAL in 1 CARTON (11994-090-06) > 24 mL in 1 VIAL
Product NDC 11994-090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Molybdenum Mo-99
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19751101
Marketing Category Name NDA
Labeler Name Lantheus Medical Imaging, Inc.
Substance Name MOLYBDENUM MO-99
Strength Number 250
Strength Unit mCi/mL
Pharmaceutical Classes

Complete Information of TechneLite


General Information