House Dust - 49643-008-10 - (House Dust)

Alphabetical Index


Drug Information of House Dust

Product NDC: 49643-008
Proprietary Name: House Dust
Non Proprietary Name: House Dust
Active Ingredient(s): 1    g/50mL & nbsp;   House Dust
Administration Route(s): CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of House Dust

Product NDC: 49643-008
Labeler Name: Allermed Laboratories, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA102212
Marketing Category: BLA
Start Marketing Date: 19740312

Package Information of House Dust

Package NDC: 49643-008-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (49643-008-10)

NDC Information of House Dust

NDC Code 49643-008-10
Proprietary Name House Dust
Package Description 10 mL in 1 VIAL, MULTI-DOSE (49643-008-10)
Product NDC 49643-008
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name House Dust
Dosage Form Name INJECTION
Route Name CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740312
Marketing Category Name BLA
Labeler Name Allermed Laboratories, Inc.
Substance Name HOUSE DUST
Strength Number 1
Strength Unit g/50mL
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