"36987-2215-4" National Drug Code (NDC)

NDC Code	36987-2215-4
Package Description	50 mL in 1 VIAL, MULTI-DOSE (36987-2215-4)
Product NDC	36987-2215
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Flaxseed
Non-Proprietary Name	Flaxseed
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19720829
Marketing Category Name	BLA
Application Number	BLA102192
Manufacturer	Nelco Laboratories, Inc.
Substance Name	FLAX SEED
Strength	10000
Strength Unit	[PNU]/mL
Pharmacy Classes	Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Seed Storage Proteins [CS]