NDC 36987-1035

Goose Feathers

Goose Feathers

Goose 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 Anser Anser Feather.

Product ID36987-1035_8f2b01b8-e712-4107-b824-e1f07faa2a41
NDC36987-1035
Product TypeHuman Prescription Drug
Proprietary NameGoose Feathers
Generic NameGoose Feathers
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1972-08-29
Marketing CategoryBLA / BLA
Application NumberBLA102192
Labeler NameNelco Laboratories, Inc.
Substance NameANSER ANSER FEATHER
Active Ingredient Strength20000 [PNU]/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 36987-1035-1

5 mL in 1 VIAL, MULTI-DOSE (36987-1035-1)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1035-1 [36987103501]

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

NDC 36987-1035-2 [36987103502]

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

NDC 36987-1035-3 [36987103503]

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

NDC 36987-1035-4 [36987103504]

Goose 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
ANSER ANSER FEATHER20000 [PNU]/mL

OpenFDA Data

SPL SET ID:001dcaf3-5838-4fb0-a4b8-d65ae2eb009e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 895193
  • 889656
  • 895308
  • 895480
  • 895079
  • 894778
  • 895069
  • 895277
  • 895298
  • 895288
  • 895470
  • 895050
  • 894928
  • 894958
  • 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 "Goose Feathers" or generic name "Goose Feathers"

    NDCBrand NameGeneric Name
    22840-1159Goose FeathersAnser anser
    22840-1160Goose FeathersAnser anser
    22840-5113Goose FeathersAnser anser
    36987-1033Goose FeathersGoose Feathers
    36987-1034Goose FeathersGoose Feathers
    36987-1035Goose FeathersGoose Feathers
    36987-1036Goose FeathersGoose Feathers
    36987-1037Goose FeathersGoose Feathers
    36987-1038Goose FeathersGoose Feathers
    36987-1039Goose FeathersGoose Feathers
    36987-1040Goose FeathersGoose Feathers
    54575-295GOOSE FEATHERSanser anser feather

    Trademark Results [Goose Feathers]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    GOOSE FEATHERS
    GOOSE FEATHERS
    78466956 not registered Dead/Abandoned
    Buzz Trading, LLC
    2004-08-13
    GOOSE FEATHERS
    GOOSE FEATHERS
    77751169 3941283 Live/Registered
    The Express Cafe & Bakery, LLC
    2009-06-03
    GOOSE FEATHERS
    GOOSE FEATHERS
    77748605 3786082 Live/Registered
    The Express Cafe & Bakery, LLC
    2009-06-01

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