Torsemide - 50111-917-03 - (Torsemide)

Alphabetical Index


Drug Information of Torsemide

Product NDC: 50111-917
Proprietary Name: Torsemide
Non Proprietary Name: Torsemide
Active Ingredient(s): 20    mg/1 & nbsp;   Torsemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Torsemide

Product NDC: 50111-917
Labeler Name: Pliva, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076346
Marketing Category: ANDA
Start Marketing Date: 20040601

Package Information of Torsemide

Package NDC: 50111-917-03
Package Description: 1000 TABLET in 1 BOTTLE (50111-917-03)

NDC Information of Torsemide

NDC Code 50111-917-03
Proprietary Name Torsemide
Package Description 1000 TABLET in 1 BOTTLE (50111-917-03)
Product NDC 50111-917
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Torsemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040601
Marketing Category Name ANDA
Labeler Name Pliva, Inc
Substance Name TORSEMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Torsemide


General Information