Furosemide - 0172-2907-10 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 0172-2907
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: 0172-2907
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018413
Marketing Category: NDA
Start Marketing Date: 19831130

Package Information of Furosemide

Package NDC: 0172-2907-10
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-2907-10) > 1 TABLET in 1 BLISTER PACK (0172-2907-00)

NDC Information of Furosemide

NDC Code 0172-2907-10
Proprietary Name Furosemide
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-2907-10) > 1 TABLET in 1 BLISTER PACK (0172-2907-00)
Product NDC 0172-2907
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19831130
Marketing Category Name NDA
Labeler Name IVAX Pharmaceuticals, 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