Furosemide - 55154-4906-0 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 55154-4906
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 20    mg/1 & nbsp;   Furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 55154-4906
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018823
Marketing Category: ANDA
Start Marketing Date: 19831110

Package Information of Furosemide

Package NDC: 55154-4906-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4906-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Furosemide

NDC Code 55154-4906-0
Proprietary Name Furosemide
Package Description 10 BLISTER PACK in 1 BAG (55154-4906-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-4906
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19831110
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name FUROSEMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information