EGG WHITE - 54575-389-10 - (egg white)

Alphabetical Index


Drug Information of EGG WHITE

Product NDC: 54575-389
Proprietary Name: EGG WHITE
Non Proprietary Name: egg white
Active Ingredient(s): 1    g/20mL & nbsp;   egg white
Administration Route(s): PERCUTANEOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of EGG WHITE

Product NDC: 54575-389
Labeler Name: Allergy Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of EGG WHITE

Package NDC: 54575-389-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (54575-389-10)

NDC Information of EGG WHITE

NDC Code 54575-389-10
Proprietary Name EGG WHITE
Package Description 10 mL in 1 VIAL, MULTI-DOSE (54575-389-10)
Product NDC 54575-389
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name egg white
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 WHITE
Strength Number 1
Strength Unit g/20mL
Pharmaceutical Classes Cell-mediated Immunity [PE],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Allergens [Chemical/Ingredient],Egg Proteins, Dietary [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient]

Complete Information of EGG WHITE


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