Furosemide - 0781-1966-01 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 0781-1966
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: 0781-1966
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018569
Marketing Category: NDA
Start Marketing Date: 19811019

Package Information of Furosemide

Package NDC: 0781-1966-01
Package Description: 100 TABLET in 1 BOTTLE (0781-1966-01)

NDC Information of Furosemide

NDC Code 0781-1966-01
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE (0781-1966-01)
Product NDC 0781-1966
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19811019
Marketing Category Name NDA
Labeler Name Sandoz 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