Furosemide - 54569-0574-0 - (furosemide)

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Drug Information of Furosemide

Product NDC: 54569-0574
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: 54569-0574
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076796
Marketing Category: ANDA
Start Marketing Date: 20040326

Package Information of Furosemide

Package NDC: 54569-0574-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54569-0574-0)

NDC Information of Furosemide

NDC Code 54569-0574-0
Proprietary Name Furosemide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54569-0574-0)
Product NDC 54569-0574
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040326
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions 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