"22840-9665-4" National Drug Code (NDC)

NDC Code	22840-9665-4
Package Description	50 mL in 1 VIAL, MULTI-DOSE (22840-9665-4)
Product NDC	22840-9665
Product Type Name	NON-STANDARDIZED ALLERGENIC
Proprietary Name	Rhizopus Mix
Non-Proprietary Name	Rhizopus Stolonifer And Rhizopus Oryzae
Dosage Form	SOLUTION
Usage	INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19810915
Marketing Category Name	BLA
Application Number	BLA101833
Manufacturer	Greer Laboratories, Inc.
Substance Name	RHIZOPUS ARRHIZUS; RHIZOPUS STOLONIFER
Strength	.025; .025
Strength Unit	g/mL; g/mL
Pharmacy Classes	Allergens [CS], Allergens [Chemical/Ingredient], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Fungal Proteins [Chemical/Ingredient], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC]