"22840-9493-4" National Drug Code (NDC)

NDC Code	22840-9493-4
Package Description	50 mL in 1 VIAL, MULTI-DOSE (22840-9493-4)
Product NDC	22840-9493
Product Type Name	NON-STANDARDIZED ALLERGENIC
Proprietary Name	Birch Pollen Mix
Non-Proprietary Name	Betula Lenta, Betula Nigra And Betula Populifolia
Dosage Form	SOLUTION
Usage	INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19810915
Marketing Category Name	BLA
Application Number	BLA101833
Manufacturer	Greer Laboratories, Inc.
Substance Name	BETULA LENTA POLLEN; BETULA NIGRA POLLEN; BETULA POPULIFOLIA POLLEN
Strength	.0166666; .0166666; .0166666
Strength Unit	g/mL; g/mL; g/mL
Pharmacy Classes	Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS], Pollen [CS], Pollen [CS]