"49643-010-30" National Drug Code (NDC)

NDC Code	49643-010-30
Package Description	30 mL in 1 VIAL, MULTI-DOSE (49643-010-30)
Product NDC	49643-010
Product Type Name	NON-STANDARDIZED ALLERGENIC
Proprietary Name	Flaxseed
Non-Proprietary Name	Flaxseed
Dosage Form	INJECTION
Usage	CUTANEOUS; INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19740312
Marketing Category Name	BLA
Application Number	BLA102211
Manufacturer	Allermed Laboratories, Inc.
Substance Name	FLAX SEED
Strength	.05
Strength Unit	g/mL
Pharmacy Classes	Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]