Bumetanide - 55154-0358-5 - (Bumetanide)

Alphabetical Index


Drug Information of Bumetanide

Product NDC: 55154-0358
Proprietary Name: Bumetanide
Non Proprietary Name: Bumetanide
Active Ingredient(s): .25    mg/mL & nbsp;   Bumetanide
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bumetanide

Product NDC: 55154-0358
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074441
Marketing Category: ANDA
Start Marketing Date: 19950301

Package Information of Bumetanide

Package NDC: 55154-0358-5
Package Description: 5 VIAL in 1 BAG (55154-0358-5) > 2 mL in 1 VIAL

NDC Information of Bumetanide

NDC Code 55154-0358-5
Proprietary Name Bumetanide
Package Description 5 VIAL in 1 BAG (55154-0358-5) > 2 mL in 1 VIAL
Product NDC 55154-0358
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bumetanide
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19950301
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name BUMETANIDE
Strength Number .25
Strength Unit mg/mL
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Bumetanide


General Information