Furosemide - 67253-541-09 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 67253-541
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: 67253-541
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018415
Marketing Category: NDA
Start Marketing Date: 19820727

Package Information of Furosemide

Package NDC: 67253-541-09
Package Description: 90 TABLET in 1 BOTTLE (67253-541-09)

NDC Information of Furosemide

NDC Code 67253-541-09
Proprietary Name Furosemide
Package Description 90 TABLET in 1 BOTTLE (67253-541-09)
Product NDC 67253-541
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820727
Marketing Category Name NDA
Labeler Name DAVA 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