"68084-016-01" National Drug Code (NDC)

NDC Code	68084-016-01
Package Description	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-016-01) > 1 TABLET in 1 BLISTER PACK (68084-016-11)
Product NDC	68084-016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Furosemide
Non-Proprietary Name	Furosemide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20060622
End Marketing Date	20150331
Marketing Category Name	ANDA
Application Number	ANDA077293
Manufacturer	American Health Packaging
Substance Name	FUROSEMIDE
Strength	40
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]