Furosemide - 54569-0570-0 - (Furosemide)

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Drug Information of Furosemide

Product NDC: 54569-0570
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 80    mg/1 & nbsp;   Furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 54569-0570
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078010
Marketing Category: ANDA
Start Marketing Date: 20090129

Package Information of Furosemide

Package NDC: 54569-0570-0
Package Description: 100 TABLET in 1 BOTTLE (54569-0570-0)

NDC Information of Furosemide

NDC Code 54569-0570-0
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE (54569-0570-0)
Product NDC 54569-0570
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090129
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name FUROSEMIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information