NDC 36987-1032

Duck Feathers

Duck Feathers

Duck Feathers 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 Anas Platyrhynchos Feather.

Product ID36987-1032_1689799a-e4a1-4882-859e-be9c4e31d6ee
NDC36987-1032
Product TypeHuman Prescription Drug
Proprietary NameDuck Feathers
Generic NameDuck Feathers
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameANAS PLATYRHYNCHOS FEATHER
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Feathers [CS],Allergens [CS],Increased IgG Production [PE]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 36987-1032-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1032-3)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1032-4 [36987103204]

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

NDC 36987-1032-3 [36987103203]

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

NDC 36987-1032-2 [36987103202]

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

NDC 36987-1032-1 [36987103201]

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

Drug Details

Active Ingredients

IngredientStrength
ANAS PLATYRHYNCHOS FEATHER.1 g/mL

OpenFDA Data

SPL SET ID:f1eabfd7-c87c-4123-822a-0bcf9f890fa2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 895075
  • 895204
  • 895065
  • 889660
  • 852696
  • 895061
  • 894749
  • 895304
  • 894917
  • 852482
  • 1006505
  • 894948
  • 852259
  • 895284
  • 895300
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Duck Feathers" or generic name "Duck Feathers"

    NDCBrand NameGeneric Name
    22840-1157Duck FeathersAnas platyrhynchos
    22840-1176Duck FeathersAnas platyrhynchos
    22840-5112Duck FeathersAnas platyrhynchos
    36987-1025Duck FeathersDuck Feathers
    36987-1026Duck FeathersDuck Feathers
    36987-1027Duck FeathersDuck Feathers
    36987-1028Duck FeathersDuck Feathers
    36987-1029Duck FeathersDuck Feathers
    36987-1030Duck FeathersDuck Feathers
    36987-1031Duck FeathersDuck Feathers
    36987-1032Duck FeathersDuck Feathers
    54575-294DUCK FEATHERSanas platyrhynchos feather

    Trademark Results [Duck Feathers]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    DUCK FEATHERS
    DUCK FEATHERS
    73499958 1354284 Dead/Cancelled
    MANI, JANET
    1984-09-18

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