NDC 36987-1880

Aspergillus repens

Aspergillus Repens

Aspergillus repens 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 Eurotium Herbariorum.

Product ID36987-1880_3fd958a1-76f3-4d4b-9233-7cf3da1c304b
NDC36987-1880
Product TypeHuman Prescription Drug
Proprietary NameAspergillus repens
Generic NameAspergillus Repens
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameEUROTIUM HERBARIORUM
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-1880-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1880-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1880-2 [36987188002]

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

NDC 36987-1880-1 [36987188001]

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

NDC 36987-1880-3 [36987188003]

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

NDC 36987-1880-4 [36987188004]

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

Drug Details

Active Ingredients

IngredientStrength
EUROTIUM HERBARIORUM.05 g/mL

OpenFDA Data

SPL SET ID:4a853ed7-32f7-44bf-bea1-3e90994e7651
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1006300
  • 1012146
  • 852041
  • 968203
  • 1006288
  • 852243
  • 314941
  • 967777
  • 968478
  • 889590
  • 1011974
  • 1011976
  • 1011972
  • 1012035
  • 1010904
  • 1012051
  • 968133
  • 1012171
  • 1006321
  • 967947
  • 967532
  • 905073
  • 966683
  • 968544
  • 852800
  • 883409
  • 968440
  • 968429
  • 967038
  • 967051
  • 1012047
  • 1012041
  • 967985
  • Pharm Class PE
  • Cell-mediated Immunity [PE]
  • Increased IgG Production [PE]
  • Increased Histamine Release [PE]
  • PHarm Class EPC
  • Non-Standardized Fungal Allergenic Extract [EPC]
  • NUI Code
  • N0000185001
  • N0000175629
  • N0000171131
  • N0000185372
  • N0000169106
  • N0000184306
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Aspergillus repens" or generic name "Aspergillus Repens"

    NDCBrand NameGeneric Name
    36987-1875Aspergillus repensAspergillus repens
    36987-1876Aspergillus repensAspergillus repens
    36987-1877Aspergillus repensAspergillus repens
    36987-1878Aspergillus repensAspergillus repens
    36987-1879Aspergillus repensAspergillus repens
    36987-1880Aspergillus repensAspergillus repens
    36987-1881Aspergillus repensAspergillus repens
    36987-1882Aspergillus repensAspergillus repens
    36987-1883Aspergillus repensAspergillus repens
    49288-0621Aspergillus repensAspergillus repens

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