"70934-111-10" National Drug Code (NDC)

NDC Code	70934-111-10
Package Description	10 TABLET in 1 BOTTLE, PLASTIC (70934-111-10)
Product NDC	70934-111
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Furosemide
Non-Proprietary Name	Furosemide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20180516
End Marketing Date	20240229
Marketing Category Name	ANDA
Application Number	ANDA077293
Manufacturer	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance Name	FUROSEMIDE
Strength	20
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]