NDC 36987-1034

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 ID36987-1034_391e0cff-b4e3-4e38-bbd8-2f9479d6998e
NDC36987-1034
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 Strength10000 [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 36987-1034-3

30 mL in 1 VIAL, MULTI-DOSE (36987-1034-3)
Marketing Start Date1972-08-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36987-1034-4 [36987103404]

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

NDC 36987-1034-3 [36987103403]

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

NDC 36987-1034-2 [36987103402]

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

NDC 36987-1034-1 [36987103401]

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 FEATHER10000 [PNU]/mL

OpenFDA Data

SPL SET ID:68a04179-30a6-4067-8585-c28e4924d578
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 895038
  • 895077
  • 894776
  • 895067
  • 889658
  • 895306
  • 895191
  • 895478
  • 895295
  • 895468
  • 894956
  • 895275
  • 894923
  • 895286
  • 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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