NDC 49288-0225

Goose Feather

Goose Feather

Goose Feather is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Anser Anser Feather.

Product ID49288-0225_f08d6882-f5d5-4109-b9df-64c85e82a0a1
NDC49288-0225
Product TypeHuman Prescription Drug
Proprietary NameGoose Feather
Generic NameGoose Feather
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameANSER ANSER 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 49288-0225-2

5 mL in 1 VIAL, MULTI-DOSE (49288-0225-2)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0225-1 [49288022501]

Goose Feather INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0225-4 [49288022504]

Goose Feather INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0225-5 [49288022505]

Goose Feather INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0225-2 [49288022502]

Goose Feather INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

NDC 49288-0225-3 [49288022503]

Goose Feather INJECTION, SOLUTION
Marketing CategoryBLA
Application NumberBLA102223
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1974-03-23
Inactivation Date2019-10-21

Drug Details

Active Ingredients

IngredientStrength
ANSER ANSER FEATHER.05 g/mL

OpenFDA Data

SPL SET ID:960c58a9-572e-41c5-8e0e-7ad1ff955030
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 895535
  • 895513
  • 894964
  • 894940
  • 895524
  • 895506
  • 894786
  • 895547
  • 895541
  • 895545
  • 895530
  • 895518
  • 895520
  • 894937
  • 895491
  • 895500
  • 895493
  • 895510
  • 895502
  • 892854
  • 895498
  • Pharmacological Class

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

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