Torsemide - 59762-1701-1 - (Torsemide)

Alphabetical Index


Drug Information of Torsemide

Product NDC: 59762-1701
Proprietary Name: Torsemide
Non Proprietary Name: Torsemide
Active Ingredient(s): 10    mg/1 & nbsp;   Torsemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Torsemide

Product NDC: 59762-1701
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078249
Marketing Category: ANDA
Start Marketing Date: 20071017

Package Information of Torsemide

Package NDC: 59762-1701-1
Package Description: 100 TABLET in 1 BOTTLE (59762-1701-1)

NDC Information of Torsemide

NDC Code 59762-1701-1
Proprietary Name Torsemide
Package Description 100 TABLET in 1 BOTTLE (59762-1701-1)
Product NDC 59762-1701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Torsemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071017
Marketing Category Name ANDA
Labeler Name Greenstone LLC
Substance Name TORSEMIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Torsemide


General Information