"49288-0912-3" National Drug Code (NDC)

NDC Code	49288-0912-3
Package Description	10 mL in 1 VIAL, MULTI-DOSE (49288-0912-3)
Product NDC	49288-0912
Product Type Name	NON-STANDARDIZED ALLERGENIC
Proprietary Name	Treatment Set Ts349357
Non-Proprietary Name	Treatment Set Ts349357
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19861031
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	AVENA SATIVA POLLEN; PHLEUM PRATENSE POLLEN; ALTERNARIA ALTERNATA; PLATANUS OCCIDENTALIS POLLEN
Strength	.002; 4000; .002; .01
Strength Unit	g/mL; [BAU]/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],Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [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]