Torsemide - 51079-026-20 - (Torsemide)

Alphabetical Index


Drug Information of Torsemide

Product NDC: 51079-026
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: 51079-026
Labeler Name: UDL Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076110
Marketing Category: ANDA
Start Marketing Date: 20100114

Package Information of Torsemide

Package NDC: 51079-026-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-026-20) > 1 TABLET in 1 BLISTER PACK (51079-026-01)

NDC Information of Torsemide

NDC Code 51079-026-20
Proprietary Name Torsemide
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-026-20) > 1 TABLET in 1 BLISTER PACK (51079-026-01)
Product NDC 51079-026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Torsemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100114
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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