"51079-073-20" National Drug Code (NDC)

NDC Code	51079-073-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-073-20) / 1 TABLET in 1 BLISTER PACK (51079-073-01)
Product NDC	51079-073
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Furosemide
Non-Proprietary Name	Furosemide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19970206
End Marketing Date	20240831
Marketing Category Name	NDA
Application Number	NDA018487
Manufacturer	Mylan Institutional Inc.
Substance Name	FUROSEMIDE
Strength	40
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]