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Goose Feathers - 36987-1039-4 - (Goose Feathers)

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Drug Information of Goose Feathers

Product NDC: 36987-1039
Proprietary Name: Goose Feathers
Non Proprietary Name: Goose Feathers
Active Ingredient(s): .1    g/mL & nbsp;   Goose Feathers
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Goose Feathers

Product NDC: 36987-1039
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Goose Feathers

Package NDC: 36987-1039-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (36987-1039-4)

NDC Information of Goose Feathers

NDC Code 36987-1039-4
Proprietary Name Goose Feathers
Package Description 50 mL in 1 VIAL, MULTI-DOSE (36987-1039-4)
Product NDC 36987-1039
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Goose Feathers
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name ANSER ANSER FEATHER
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Feather Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Feathers [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Goose Feathers


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