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BOTRYTIS CINEREA - 0268-0837-50 - (BOTRYTIS CINEREA)

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Drug Information of BOTRYTIS CINEREA

Product NDC: 0268-0837
Proprietary Name: BOTRYTIS CINEREA
Non Proprietary Name: BOTRYTIS CINEREA
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   BOTRYTIS CINEREA
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of BOTRYTIS CINEREA

Product NDC: 0268-0837
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of BOTRYTIS CINEREA

Package NDC: 0268-0837-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0837-50)

NDC Information of BOTRYTIS CINEREA

NDC Code 0268-0837-50
Proprietary Name BOTRYTIS CINEREA
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0837-50)
Product NDC 0268-0837
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name BOTRYTIS CINEREA
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name BOTRYTIS CINEREA
Strength Number 20000
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 BOTRYTIS CINEREA


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