Furosemide - 0378-0232-01 - (furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 0378-0232
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: 0378-0232
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070082
Marketing Category: ANDA
Start Marketing Date: 19870827

Package Information of Furosemide

Package NDC: 0378-0232-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0232-01)

NDC Information of Furosemide

NDC Code 0378-0232-01
Proprietary Name Furosemide
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0232-01)
Product NDC 0378-0232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870827
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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