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Parakeet Feather - 49288-0390-1 - (Parakeet Feather)

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Drug Information of Parakeet Feather

Product NDC: 49288-0390
Proprietary Name: Parakeet Feather
Non Proprietary Name: Parakeet Feather
Active Ingredient(s): .02    g/mL & nbsp;   Parakeet Feather
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Parakeet Feather

Product NDC: 49288-0390
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Parakeet Feather

Package NDC: 49288-0390-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0390-1)

NDC Information of Parakeet Feather

NDC Code 49288-0390-1
Proprietary Name Parakeet Feather
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0390-1)
Product NDC 49288-0390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Parakeet Feather
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19740323
Marketing Category Name BLA
Labeler Name Antigen Laboratories, Inc.
Substance Name MELOPSITTACUS UNDULATUS FEATHER
Strength Number .02
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Feathers [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Feathers [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Parakeet Feather


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