"36987-3220-1" National Drug Code (NDC)

NDC Code	36987-3220-1
Package Description	5 mL in 1 VIAL, MULTI-DOSE (36987-3220-1)
Product NDC	36987-3220
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Western Water Hemp
Non-Proprietary Name	Western Water Hemp
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19720829
Marketing Category Name	BLA
Application Number	BLA102192
Manufacturer	Nelco Laboratories, Inc.
Substance Name	AMARANTHUS TUBERCULATUS POLLEN
Strength	.1
Strength Unit	g/mL
Pharmacy Classes	Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [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]