"0781-1446-05" National Drug Code (NDC)

NDC Code	0781-1446-05
Package Description	500 TABLET in 1 BOTTLE (0781-1446-05)
Product NDC	0781-1446
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	20211130
Marketing Category Name	NDA
Application Number	NDA018569
Manufacturer	Sandoz Inc
Substance Name	FUROSEMIDE
Strength	80
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]