"70702-001-50" National Drug Code (NDC)

NDC Code	70702-001-50
Package Description	500 TABLET in 1 BOTTLE (70702-001-50)
Product NDC	70702-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bumetanide
Non-Proprietary Name	Bumetanide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20160809
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA018225
Manufacturer	Paragon Enterprises, Inc
Substance Name	BUMETANIDE
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]