Furosemide - 0603-3741-04 - (furosemide)

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Drug Information of Furosemide

Product NDC: 0603-3741
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: 0603-3741
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076796
Marketing Category: ANDA
Start Marketing Date: 20040326

Package Information of Furosemide

Package NDC: 0603-3741-04
Package Description: 180 TABLET in 1 BOTTLE, PLASTIC (0603-3741-04)

NDC Information of Furosemide

NDC Code 0603-3741-04
Proprietary Name Furosemide
Package Description 180 TABLET in 1 BOTTLE, PLASTIC (0603-3741-04)
Product NDC 0603-3741
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 Qualitest Pharmaceuticals
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