Egg White - 36987-1130-1 - (Egg White)

Alphabetical Index


Drug Information of Egg White

Product NDC: 36987-1130
Proprietary Name: Egg White
Non Proprietary Name: Egg White
Active Ingredient(s): .05    g/mL & nbsp;   Egg White
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Egg White

Product NDC: 36987-1130
Labeler Name: Nelco 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: 36987-1130-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (36987-1130-1)

NDC Information of Egg White

NDC Code 36987-1130-1
Proprietary Name Egg White
Package Description 5 mL in 1 VIAL, MULTI-DOSE (36987-1130-1)
Product NDC 36987-1130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Egg White
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name EGG WHITE
Strength Number .05
Strength Unit g/mL
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


General Information