NDC 49288-0315

Mattress Dust

Mattress Dust

Mattress 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 ID49288-0315_89b69938-05fc-4bd8-9c55-4fb46e9018c7
NDC49288-0315
Product TypeHuman Prescription Drug
Proprietary NameMattress Dust
Generic NameMattress 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 49288-0315-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0315-3)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0315-4 [49288031504]

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

NDC 49288-0315-2 [49288031502]

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

NDC 49288-0315-1 [49288031501]

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

NDC 49288-0315-5 [49288031505]

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

NDC 49288-0315-3 [49288031503]

Mattress 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.05 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]

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