Furosemide - 51079-073-56 - (furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 51079-073
Proprietary Name: Furosemide
Non Proprietary Name: furosemide
Active Ingredient(s): 40    mg/1 & nbsp;   furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 51079-073
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018487
Marketing Category: NDA
Start Marketing Date: 20101012

Package Information of Furosemide

Package NDC: 51079-073-56
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-073-56) > 30 TABLET in 1 BLISTER PACK (51079-073-30)

NDC Information of Furosemide

NDC Code 51079-073-56
Proprietary Name Furosemide
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-073-56) > 30 TABLET in 1 BLISTER PACK (51079-073-30)
Product NDC 51079-073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101012
Marketing Category Name NDA
Labeler Name UDL Laboratories, Inc.
Substance Name FUROSEMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information