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USTILAGO TRITICI - 0268-0952-10 - (LOOSE WHEAT SMUT)

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Drug Information of USTILAGO TRITICI

Product NDC: 0268-0952
Proprietary Name: USTILAGO TRITICI
Non Proprietary Name: LOOSE WHEAT SMUT
Active Ingredient(s): .05    g/mL & nbsp;   LOOSE WHEAT SMUT
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of USTILAGO TRITICI

Product NDC: 0268-0952
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of USTILAGO TRITICI

Package NDC: 0268-0952-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (0268-0952-10)

NDC Information of USTILAGO TRITICI

NDC Code 0268-0952-10
Proprietary Name USTILAGO TRITICI
Package Description 10 mL in 1 VIAL, MULTI-DOSE (0268-0952-10)
Product NDC 0268-0952
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name LOOSE WHEAT SMUT
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name USTILAGO TRITICI
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of USTILAGO TRITICI


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