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Canary Feather - 49288-0127-1 - (Canary Feather)

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Drug Information of Canary Feather

Product NDC: 49288-0127
Proprietary Name: Canary Feather
Non Proprietary Name: Canary Feather
Active Ingredient(s): .02    g/mL & nbsp;   Canary Feather
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Canary Feather

Product NDC: 49288-0127
Labeler Name: Antigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102223
Marketing Category: BLA
Start Marketing Date: 19740323

Package Information of Canary Feather

Package NDC: 49288-0127-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (49288-0127-1)

NDC Information of Canary Feather

NDC Code 49288-0127-1
Proprietary Name Canary Feather
Package Description 2 mL in 1 VIAL, MULTI-DOSE (49288-0127-1)
Product NDC 49288-0127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Canary 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 SERINUS CANARIA FEATHER
Strength Number .02
Strength Unit g/mL
Pharmaceutical Classes Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Feathers [Chemical/Ingredient],Non-Standardized Feather Allergenic Extract [EPC],Allergens [Chemical/Ingredient]

Complete Information of Canary Feather


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