Furosemide - 52125-466-02 - (Furosemide)

Alphabetical Index


Drug Information of Furosemide

Product NDC: 52125-466
Proprietary Name: Furosemide
Non Proprietary Name: Furosemide
Active Ingredient(s): 20    mg/1 & nbsp;   Furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 52125-466
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018413
Marketing Category: NDA
Start Marketing Date: 20130522

Package Information of Furosemide

Package NDC: 52125-466-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-466-02)

NDC Information of Furosemide

NDC Code 52125-466-02
Proprietary Name Furosemide
Package Description 30 TABLET in 1 BLISTER PACK (52125-466-02)
Product NDC 52125-466
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name FUROSEMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information