NDC 36987-1870

Aspergillus flavus

Aspergillus Flavus

Aspergillus flavus 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 Aspergillus Flavus.

Product ID36987-1870_9010bf62-c443-49a9-b8f8-fa8dd9223885
NDC36987-1870
Product TypeHuman Prescription Drug
Proprietary NameAspergillus flavus
Generic NameAspergillus Flavus
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameASPERGILLUS FLAVUS
Active Ingredient Strength40000 [PNU]/mL
Pharm ClassesNon-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Fungal Proteins [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-1870-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1870-2)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1870-4 [36987187004]

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

NDC 36987-1870-2 [36987187002]

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

NDC 36987-1870-3 [36987187003]

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

NDC 36987-1870-1 [36987187001]

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

Drug Details

Active Ingredients

IngredientStrength
ASPERGILLUS FLAVUS40000 [PNU]/mL

OpenFDA Data

SPL SET ID:8559987a-4127-45d1-81c8-9bce75e85db3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1006305
  • 967955
  • 968200
  • 967545
  • 967910
  • 1011993
  • 1012320
  • 889536
  • 1012106
  • 966960
  • 307874
  • 968458
  • 889577
  • 1010862
  • 1010908
  • 968486
  • 1012053
  • 967047
  • 1012154
  • 1012039
  • 1012037
  • 1006337
  • 1012174
  • 1006294
  • 889606
  • 966691
  • 968540
  • 966668
  • 967059
  • 905081
  • 1012049
  • 968153
  • 1012045
  • 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]
    • Fungal Proteins [CS]
    • Allergens [CS]

    NDC Crossover Matching brand name "Aspergillus flavus" or generic name "Aspergillus Flavus"

    NDCBrand NameGeneric Name
    22840-1610Aspergillus flavusAspergillus flavus
    22840-1612Aspergillus flavusAspergillus flavus
    22840-1614Aspergillus flavusAspergillus flavus
    22840-5603Aspergillus flavusAspergillus flavus
    36987-1866Aspergillus flavusAspergillus flavus
    36987-1867Aspergillus flavusAspergillus flavus
    36987-1868Aspergillus flavusAspergillus flavus
    36987-1869Aspergillus flavusAspergillus flavus
    36987-1870Aspergillus flavusAspergillus flavus
    36987-1871Aspergillus flavusAspergillus flavus
    36987-1872Aspergillus flavusAspergillus flavus
    36987-1873Aspergillus flavusAspergillus flavus
    36987-1874Aspergillus flavusAspergillus flavus
    49288-0624Aspergillus flavusAspergillus flavus

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