"49288-0611-4" National Drug Code (NDC)

NDC Code	49288-0611-4
Package Description	30 mL in 1 VIAL, MULTI-DOSE (49288-0611-4)
Product NDC	49288-0611
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Number Two Weed Mixture
Non-Proprietary Name	Number Two Weed Mixture
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19740323
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	XANTHIUM STRUMARIUM POLLEN; CHENOPODIUM ALBUM POLLEN; AMARANTHUS RETROFLEXUS POLLEN; RUMEX ACETOSELLA POLLEN; RUMEX CRISPUS POLLEN
Strength	.01; .01; .01; .01; .01
Strength Unit	g/mL; 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],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]