"49288-0311-2" National Drug Code (NDC)

NDC Code	49288-0311-2
Package Description	5 mL in 1 VIAL, MULTI-DOSE (49288-0311-2)
Product NDC	49288-0311
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Mulberry Mixture
Non-Proprietary Name	Mulberry 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	BROUSSONETIA PAPYRIFERA POLLEN; MORUS RUBRA POLLEN; MORUS ALBA POLLEN
Strength	.0167; .0167; .0167
Strength Unit	g/mL; g/mL; g/mL
Pharmacy Classes	Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],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]