Furosemide - 0054-4301-25 - (Furosemide)

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Drug Information of Furosemide

Product NDC: 0054-4301
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: 0054-4301
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070086
Marketing Category: ANDA
Start Marketing Date: 19910313

Package Information of Furosemide

Package NDC: 0054-4301-25
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)

NDC Information of Furosemide

NDC Code 0054-4301-25
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)
Product NDC 0054-4301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19910313
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc
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