Furosemide - 50742-104-10 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 50742-104
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 20    mg/1 & nbsp;   Furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 50742-104
Labeler Name: Ingenus Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078010
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Furosemide

Package NDC: 50742-104-10
Package Description: 1000 TABLET in 1 BOTTLE (50742-104-10)

NDC Information of Furosemide

NDC Code 50742-104-10
Proprietary Name Furosemide
Package Description 1000 TABLET in 1 BOTTLE (50742-104-10)
Product NDC 50742-104
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name Ingenus Pharmaceuticals, LLC
Substance Name FUROSEMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information