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MUCOR PLUMBEUS - 0268-0913-50 - (MUCOR PLUMBEUS)

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Drug Information of MUCOR PLUMBEUS

Product NDC: 0268-0913
Proprietary Name: MUCOR PLUMBEUS
Non Proprietary Name: MUCOR PLUMBEUS
Active Ingredient(s): 40000    [PNU]/mL & nbsp;   MUCOR PLUMBEUS
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MUCOR PLUMBEUS

Product NDC: 0268-0913
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of MUCOR PLUMBEUS

Package NDC: 0268-0913-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0913-50)

NDC Information of MUCOR PLUMBEUS

NDC Code 0268-0913-50
Proprietary Name MUCOR PLUMBEUS
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0913-50)
Product NDC 0268-0913
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name MUCOR PLUMBEUS
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name MUCOR PLUMBEUS
Strength Number 40000
Strength Unit [PNU]/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 MUCOR PLUMBEUS


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