"49288-0117-1" National Drug Code (NDC)

NDC Code	49288-0117-1
Package Description	2 mL in 1 VIAL, MULTI-DOSE (49288-0117-1)
Product NDC	49288-0117
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cranberry
Non-Proprietary Name	Cranberry
Dosage Form	INJECTION, SOLUTION
Usage	INTRADERMAL; SUBCUTANEOUS
Start Marketing Date	19740323
Marketing Category Name	BLA
Application Number	BLA102223
Manufacturer	Antigen Laboratories, Inc.
Substance Name	CRANBERRY
Strength	.05
Strength Unit	g/mL
Pharmacy Classes	Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Non-Standardized Food Allergenic Extract [EPC],Fruit Proteins [EXT]