"49643-501-30" National Drug Code (NDC)

NDC Code	49643-501-30
Package Description	30 mL in 1 VIAL, MULTI-DOSE (49643-501-30)
Product NDC	49643-501
Product Type Name	NON-STANDARDIZED ALLERGENIC
Proprietary Name	Alder Mix
Non-Proprietary Name	Alnus Rhombifolia/alnus Rubra/alnus Rugosa
Dosage Form	LIQUID
Usage	PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19740312
Marketing Category Name	BLA
Application Number	BLA102211
Manufacturer	Allermed Laboratories, Inc.
Substance Name	ALNUS INCANA SUBSP. RUGOSA POLLEN; ALNUS RHOMBIFOLIA POLLEN; ALNUS RUBRA POLLEN
Strength	.0167; .0167; .0167
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]