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AUREOBASIDIUM PULLULANS VAR PULLULANS - 0268-0836-50 - (PULLULARIA PULLULANS)

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Drug Information of AUREOBASIDIUM PULLULANS VAR PULLULANS

Product NDC: 0268-0836
Proprietary Name: AUREOBASIDIUM PULLULANS VAR PULLULANS
Non Proprietary Name: PULLULARIA PULLULANS
Active Ingredient(s): 10000    [PNU]/mL & nbsp;   PULLULARIA PULLULANS
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AUREOBASIDIUM PULLULANS VAR PULLULANS

Product NDC: 0268-0836
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of AUREOBASIDIUM PULLULANS VAR PULLULANS

Package NDC: 0268-0836-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0836-50)

NDC Information of AUREOBASIDIUM PULLULANS VAR PULLULANS

NDC Code 0268-0836-50
Proprietary Name AUREOBASIDIUM PULLULANS VAR PULLULANS
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0836-50)
Product NDC 0268-0836
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name PULLULARIA PULLULANS
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name AUREOBASIDIUM PULLULANS VAR. PULLUTANS
Strength Number 10000
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 AUREOBASIDIUM PULLULANS VAR PULLULANS


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