Furosemide - 68788-9778-1 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 68788-9778
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: 68788-9778
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078010
Marketing Category: ANDA
Start Marketing Date: 20120725

Package Information of Furosemide

Package NDC: 68788-9778-1
Package Description: 100 TABLET in 1 BOTTLE (68788-9778-1)

NDC Information of Furosemide

NDC Code 68788-9778-1
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE (68788-9778-1)
Product NDC 68788-9778
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120725
Marketing Category Name ANDA
Labeler Name Preferred 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