"48951-3200-1" National Drug Code (NDC)

NDC Code	48951-3200-1
Package Description	10 BLISTER PACK in 1 BOX (48951-3200-1) > 2 g in 1 BLISTER PACK
Product NDC	48951-3200
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cartilago Betula Adult Size Special Order
Non-Proprietary Name	Cartilago Betula Adult Size Special Order
Dosage Form	SUPPOSITORY
Usage	RECTAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	BETULA PUBESCENS LEAF; BOS TAURUS CARTILAGE; FORMICA RUFA; GOLD; ONION; TIN
Strength	5; 6; 15; 10; 15; 8
Strength Unit	[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacy Classes	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]