"49288-0616-2" National Drug Code (NDC)

NDC Code	49288-0616-2
Package Description	5 mL in 1 VIAL, MULTI-DOSE (49288-0616-2)
Product NDC	49288-0616
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Number Three Weed Mixture
Non-Proprietary Name	Number Three Weed Mixture
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19960711
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	KOCHIA SCOPARIA POLLEN; CHENOPODIUM ALBUM POLLEN; AMARANTHUS RETROFLEXUS POLLEN; RUMEX ACETOSELLA POLLEN
Strength	.0125; .0125; .0125; .0125
Strength Unit	g/mL; g/mL; g/mL; g/mL
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],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS]