Furosemide - 49999-030-00 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 49999-030
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: 49999-030
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018569
Marketing Category: ANDA
Start Marketing Date: 20111128

Package Information of Furosemide

Package NDC: 49999-030-00
Package Description: 100 TABLET in 1 BOTTLE (49999-030-00)

NDC Information of Furosemide

NDC Code 49999-030-00
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE (49999-030-00)
Product NDC 49999-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111128
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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