Bumetanide - 54868-4352-0 - (Bumetanide)

Alphabetical Index


Drug Information of Bumetanide

Product NDC: 54868-4352
Proprietary Name: Bumetanide
Non Proprietary Name: Bumetanide
Active Ingredient(s): 2    mg/1 & nbsp;   Bumetanide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bumetanide

Product NDC: 54868-4352
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074700
Marketing Category: ANDA
Start Marketing Date: 20061213

Package Information of Bumetanide

Package NDC: 54868-4352-0
Package Description: 30 TABLET in 1 BOTTLE (54868-4352-0)

NDC Information of Bumetanide

NDC Code 54868-4352-0
Proprietary Name Bumetanide
Package Description 30 TABLET in 1 BOTTLE (54868-4352-0)
Product NDC 54868-4352
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bumetanide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061213
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name BUMETANIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Bumetanide


General Information