WHOLE EGG - 54575-390-02 - (egg)

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Drug Information of WHOLE EGG

Product NDC: 54575-390
Proprietary Name: WHOLE EGG
Non Proprietary Name: egg
Active Ingredient(s): 1    g/20mL & nbsp;   egg
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of WHOLE EGG

Product NDC: 54575-390
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of WHOLE EGG

Package NDC: 54575-390-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE (54575-390-02)

NDC Information of WHOLE EGG

NDC Code 54575-390-02
Proprietary Name WHOLE EGG
Package Description 2 mL in 1 VIAL, MULTI-DOSE (54575-390-02)
Product NDC 54575-390
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name egg
Dosage Form Name INJECTION, SOLUTION
Route Name PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Allergy Laboratories, Inc.
Substance Name EGG
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Egg Proteins, Dietary [Chemical/Ingredient]

Complete Information of WHOLE EGG


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