NDC 49288-0180

A. Dust

House Dust

A. Dust is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is House Dust.

Product ID49288-0180_89b69938-05fc-4bd8-9c55-4fb46e9018c7
NDC49288-0180
Product TypeHuman Prescription Drug
Proprietary NameA. Dust
Generic NameHouse Dust
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameHOUSE DUST
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],House Dust [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0180-1

2 mL in 1 VIAL, MULTI-DOSE (49288-0180-1)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0180-4 [49288018004]

A. Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0180-2 [49288018002]

A. Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0180-1 [49288018001]

A. Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0180-3 [49288018003]

A. Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0180-5 [49288018005]

A. Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
HOUSE DUST.1 g/mL

OpenFDA Data

SPL SET ID:1a99af9f-2e6b-432b-8fe5-a40dc468242b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 901358
  • 901360
  • Pharmacological Class

    • Non-Standardized House Dust Allergenic Extract [EPC]
    • Increased Histamine Release [PE]
    • Cell-mediated Immunity [PE]
    • Increased IgG Production [PE]
    • Allergens [CS]
    • House Dust [CS]

    NDC Crossover Matching brand name "A. Dust" or generic name "House Dust"

    NDCBrand NameGeneric Name
    49288-0180A. DustHouse Dust
    49288-0181A. DustHouse Dust
    58264-0301A-9House dust
    36987-1122House DustHouse Dust
    36987-1123House DustHouse Dust
    36987-1124House DustHouse Dust
    36987-1125House DustHouse Dust
    36987-1126House DustHouse Dust
    36987-1127House DustHouse Dust
    36987-1128House DustHouse Dust
    36987-1129House DustHouse Dust
    49643-008House DustHouse Dust
    54575-267HOUSE DUSThouse dust

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