A. Dust - 49288-0181-2 - (House Dust)

Alphabetical Index


Drug Information of A. Dust

Product NDC: 49288-0181
Proprietary Name: A. Dust
Non Proprietary Name: House Dust
Active Ingredient(s): .05    g/mL & nbsp;   House Dust
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of A. Dust

Product NDC: 49288-0181
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of A. Dust

Package NDC: 49288-0181-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (49288-0181-2)

NDC Information of A. Dust

NDC Code 49288-0181-2
Proprietary Name A. Dust
Package Description 5 mL in 1 VIAL, MULTI-DOSE (49288-0181-2)
Product NDC 49288-0181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name House Dust
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, 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 A. Dust


General Information