NDC 49288-0390

Parakeet Feather

Parakeet Feather

Parakeet 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 Melopsittacus Undulatus Feather.

Product ID49288-0390_1d474d27-4ce9-4bf6-b468-4a92281edc72
NDC49288-0390
Product TypeHuman Prescription Drug
Proprietary NameParakeet Feather
Generic NameParakeet Feather
Dosage FormInjection, Solution
Route of AdministrationINTRADERMAL; SUBCUTANEOUS
Marketing Start Date1974-03-23
Marketing CategoryBLA / BLA
Application NumberBLA102223
Labeler NameAntigen Laboratories, Inc.
Substance NameMELOPSITTACUS UNDULATUS FEATHER
Active Ingredient Strength0 g/mL
Pharm ClassesNon-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Feathers [CS],Allergens [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 49288-0390-4

30 mL in 1 VIAL, MULTI-DOSE (49288-0390-4)
Marketing Start Date1974-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49288-0390-1 [49288039001]

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

NDC 49288-0390-5 [49288039005]

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

NDC 49288-0390-4 [49288039004]

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

NDC 49288-0390-2 [49288039002]

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

NDC 49288-0390-3 [49288039003]

Parakeet 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
MELOPSITTACUS UNDULATUS FEATHER.02 g/mL

OpenFDA Data

SPL SET ID:eb2f0512-0060-4508-a4ea-2ddd73396cdd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1192991
  • Pharmacological Class

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

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