Furosemide - 63739-111-01 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 63739-111
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: 63739-111
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018569
Marketing Category: ANDA
Start Marketing Date: 20041001

Package Information of Furosemide

Package NDC: 63739-111-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-111-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of Furosemide

NDC Code 63739-111-01
Proprietary Name Furosemide
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-111-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-111
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041001
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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