NDC 36987-1128

House Dust

House Dust

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

Product ID36987-1128_0dacbc5b-587a-4c20-ad07-45caf841a3ba
NDC36987-1128
Product TypeHuman Prescription Drug
Proprietary NameHouse Dust
Generic NameHouse Dust
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco 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 36987-1128-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1128-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1128-2 [36987112802]

House Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-1128-1 [36987112801]

House Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-1128-4 [36987112804]

House Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

NDC 36987-1128-3 [36987112803]

House Dust INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102192
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1972-08-29
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
HOUSE DUST.05 g/mL

OpenFDA Data

SPL SET ID:d47f69c2-ff46-48fa-9398-aeab1496b6bb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 901358
  • 307923
  • 307922
  • 901360
  • 307924
  • 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 "House Dust" or generic name "House Dust"

    NDCBrand NameGeneric Name
    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
    58264-0301A-9House dust
    49288-0180A. DustHouse Dust
    49288-0181A. DustHouse Dust

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.