"48951-8174-1" National Drug Code (NDC)

NDC Code	48951-8174-1
Package Description	10 AMPULE in 1 BOX (48951-8174-1) > 1 mL in 1 AMPULE
Product NDC	48951-8174
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Secale Betula Special Order
Non-Proprietary Name	Secale Betula Special Order
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	BETULA PUBESCENS LEAF; BETULA PUBESCENS BARK; LEVISTICUM OFFICINALE ROOT; TOBACCO LEAF; CLAVICEPS PURPUREA SCLEROTIUM; LEAD SULFIDE; BOS TAURUS EYE; ARNICA MONTANA
Strength	3; 4; 6; 6; 6; 8; 8; 12
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL