"49288-0183-5" National Drug Code (NDC)

NDC Code	49288-0183-5
Package Description	50 mL in 1 VIAL, MULTI-DOSE (49288-0183-5)
Product NDC	49288-0183
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dock/sorrel Mixture
Non-Proprietary Name	Dock/sorrel Mixture
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	20070716
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	RUMEX CRISPUS POLLEN; RUMEX ACETOSELLA POLLEN
Strength	.025; .025
Strength Unit	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],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS]