Furosemide - 52125-531-20 - (furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 52125-531
Proprietary Name: Furosemide
Non Proprietary Name: furosemide
Active Ingredient(s): 40    mg/1 & nbsp;   furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 52125-531
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018487
Marketing Category: NDA
Start Marketing Date: 20130523

Package Information of Furosemide

Package NDC: 52125-531-20
Package Description: 100 TABLET in 1 VIAL (52125-531-20)

NDC Information of Furosemide

NDC Code 52125-531-20
Proprietary Name Furosemide
Package Description 100 TABLET in 1 VIAL (52125-531-20)
Product NDC 52125-531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name FUROSEMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information