"54575-259-30" National Drug Code (NDC)

NDC Code	54575-259-30
Package Description	30 mL in 1 VIAL, MULTI-DOSE (54575-259-30)
Product NDC	54575-259
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Flax Seed For Diagnostic Use Only
Non-Proprietary Name	Flax Seed
Dosage Form	INJECTION, SOLUTION
Usage	PERCUTANEOUS; SUBCUTANEOUS
Start Marketing Date	19671207
Marketing Category Name	BLA
Application Number	BLA101376
Manufacturer	Allergy Laboratories, Inc.
Substance Name	FLAX SEED
Strength	1
Strength Unit	g/20mL
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]