"54575-468-50" National Drug Code (NDC)

NDC Code	54575-468-50
Package Description	50 mL in 1 VIAL, MULTI-DOSE (54575-468-50)
Product NDC	54575-468
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tuna
Non-Proprietary Name	Tuna
Dosage Form	INJECTION, SOLUTION
Usage	PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19720829
Marketing Category Name	BLA
Application Number	BLA102192
Manufacturer	Allergy Laboratories, Inc.
Substance Name	TUNA
Strength	1
Strength Unit	g/20mL
Pharmacy Classes	Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Fish Proteins, Dietary [EXT]