"54575-913-50" National Drug Code (NDC)

NDC Code	54575-913-50
Package Description	50 mL in 1 VIAL, MULTI-DOSE (54575-913-50)
Product NDC	54575-913
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Birch Mix, River/paper/sweet/white Pollen
Non-Proprietary Name	Betula Nigra Pollen And Betula Papyrifera Pollen And Betula Lenta Pollen And Betula Populifolia Pollen
Dosage Form	INJECTION, SOLUTION
Usage	PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19671207
Marketing Category Name	BLA
Application Number	BLA101376
Manufacturer	Allergy Laboratories, Inc.
Substance Name	BETULA NIGRA POLLEN; BETULA PAPYRIFERA POLLEN; BETULA LENTA POLLEN; BETULA POPULIFOLIA POLLEN
Strength	.25; .25; .25; .25
Strength Unit	g/20mL; g/20mL; g/20mL; g/20mL
Pharmacy Classes	Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Non-Standardized Pollen Allergenic Extract [EPC],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]