Bumetanide - 50436-4234-1 - (Bumetanide)

Alphabetical Index


Drug Information of Bumetanide

Product NDC: 50436-4234
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: 50436-4234
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074225
Marketing Category: ANDA
Start Marketing Date: 20071016

Package Information of Bumetanide

Package NDC: 50436-4234-1
Package Description: 30 TABLET in 1 BOTTLE (50436-4234-1)

NDC Information of Bumetanide

NDC Code 50436-4234-1
Proprietary Name Bumetanide
Package Description 30 TABLET in 1 BOTTLE (50436-4234-1)
Product NDC 50436-4234
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bumetanide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071016
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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