HOUSE DUST - 0268-0013-50 - (House Dust)

Alphabetical Index


Drug Information of HOUSE DUST

Product NDC: 0268-0013
Proprietary Name: HOUSE DUST
Non Proprietary Name: House Dust
Active Ingredient(s): .05    g/mL & nbsp;   House Dust
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HOUSE DUST

Product NDC: 0268-0013
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of HOUSE DUST

Package NDC: 0268-0013-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0013-50)

NDC Information of HOUSE DUST

NDC Code 0268-0013-50
Proprietary Name HOUSE DUST
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0013-50)
Product NDC 0268-0013
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name House Dust
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name HOUSE DUST
Strength Number .05
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],House Dust [Chemical/Ingredient]

Complete Information of HOUSE DUST


General Information