"49288-0052-5" National Drug Code (NDC)

NDC Code	49288-0052-5
Package Description	50 mL in 1 VIAL, MULTI-DOSE (49288-0052-5)
Product NDC	49288-0052
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Beet
Non-Proprietary Name	Beet
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19740323
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	BEET
Strength	.05
Strength Unit	g/mL
Pharmacy Classes	Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Vegetable Proteins [CS]