"0781-1966-01" National Drug Code (NDC)

NDC Code	0781-1966-01
Package Description	100 TABLET in 1 BOTTLE (0781-1966-01)
Product NDC	0781-1966
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Furosemide
Non-Proprietary Name	Furosemide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19811019
End Marketing Date	20201130
Marketing Category Name	NDA
Application Number	NDA018569
Manufacturer	Sandoz Inc
Substance Name	FUROSEMIDE
Strength	40
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]