Furosemide - 67046-221-30 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 67046-221
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: 67046-221
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA018413
Marketing Category: ANDA
Start Marketing Date: 20110208

Package Information of Furosemide

Package NDC: 67046-221-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-221-30)

NDC Information of Furosemide

NDC Code 67046-221-30
Proprietary Name Furosemide
Package Description 30 TABLET in 1 BLISTER PACK (67046-221-30)
Product NDC 67046-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110208
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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