"49288-0843-3" National Drug Code (NDC)

NDC Code	49288-0843-3
Package Description	10 mL in 1 VIAL, MULTI-DOSE (49288-0843-3)
Product NDC	49288-0843
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Treatment Set Ts345268
Non-Proprietary Name	Treatment Set Ts345268
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19861031
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	AMBROSIA ARTEMISIIFOLIA POLLEN; AMBROSIA TRIFIDA POLLEN
Strength	20000; .01
Strength Unit	[AU]/mL; g/mL
Pharmacy Classes	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]