HOUSE DUST - 54575-267-02 - (house dust)

Alphabetical Index


Drug Information of HOUSE DUST

Product NDC: 54575-267
Proprietary Name: HOUSE DUST
Non Proprietary Name: house dust
Active Ingredient(s): 1    g/20mL & nbsp;   house dust
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HOUSE DUST

Product NDC: 54575-267
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA101376
Marketing Category: BLA
Start Marketing Date: 19671207

Package Information of HOUSE DUST

Package NDC: 54575-267-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-267-02)

NDC Information of HOUSE DUST

NDC Code 54575-267-02
Proprietary Name HOUSE DUST
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-267-02)
Product NDC 54575-267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name house dust
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19671207
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name HOUSE DUST
Strength Number 1
Strength Unit g/20mL
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