Torsemide - 68084-539-01 - (Torsemide)

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Drug Information of Torsemide

Product NDC: 68084-539
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: 68084-539
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079234
Marketing Category: ANDA
Start Marketing Date: 20130702

Package Information of Torsemide

Package NDC: 68084-539-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-539-01) > 10 TABLET in 1 BLISTER PACK (68084-539-11)

NDC Information of Torsemide

NDC Code 68084-539-01
Proprietary Name Torsemide
Package Description 10 BLISTER PACK in 1 CARTON (68084-539-01) > 10 TABLET in 1 BLISTER PACK (68084-539-11)
Product NDC 68084-539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Torsemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130702
Marketing Category Name ANDA
Labeler Name American Health Packaging
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