Bumetanide - 0409-1412-49 - (BUMETANIDE)

Alphabetical Index


Drug Information of Bumetanide

Product NDC: 0409-1412
Proprietary Name: Bumetanide
Non Proprietary Name: BUMETANIDE
Active Ingredient(s): .25    mg/mL & nbsp;   BUMETANIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Bumetanide

Product NDC: 0409-1412
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074332
Marketing Category: ANDA
Start Marketing Date: 20111116

Package Information of Bumetanide

Package NDC: 0409-1412-49
Package Description: 10 VIAL in 1 BOX (0409-1412-49) > 4 mL in 1 VIAL

NDC Information of Bumetanide

NDC Code 0409-1412-49
Proprietary Name Bumetanide
Package Description 10 VIAL in 1 BOX (0409-1412-49) > 4 mL in 1 VIAL
Product NDC 0409-1412
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BUMETANIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20111116
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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