"48951-4049-1" National Drug Code (NDC)

NDC Code	48951-4049-1
Package Description	10 AMPULE in 1 BOX (48951-4049-1) > 1 mL in 1 AMPULE
Product NDC	48951-4049
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Eupatorium Comp.
Non-Proprietary Name	Eupatorium Comp.
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; LACHESIS MUTA VENOM; PHOSPHORUS
Strength	6; 6; 5; 12; 7
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL