Furosemide - 43063-075-60 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 43063-075
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: 43063-075
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077293
Marketing Category: ANDA
Start Marketing Date: 20060201

Package Information of Furosemide

Package NDC: 43063-075-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (43063-075-60)

NDC Information of Furosemide

NDC Code 43063-075-60
Proprietary Name Furosemide
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (43063-075-60)
Product NDC 43063-075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060201
Marketing Category Name ANDA
Labeler Name PD-Rx 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