EDECRIN - 0179-0126-70 - (ethacrynic acid)

Alphabetical Index


Drug Information of EDECRIN

Product NDC: 0179-0126
Proprietary Name: EDECRIN
Non Proprietary Name: ethacrynic acid
Active Ingredient(s): 25    mg/1 & nbsp;   ethacrynic acid
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of EDECRIN

Product NDC: 0179-0126
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016092
Marketing Category: NDA
Start Marketing Date: 20130110

Package Information of EDECRIN

Package NDC: 0179-0126-70
Package Description: 30 TABLET in 1 BOX, UNIT-DOSE (0179-0126-70)

NDC Information of EDECRIN

NDC Code 0179-0126-70
Proprietary Name EDECRIN
Package Description 30 TABLET in 1 BOX, UNIT-DOSE (0179-0126-70)
Product NDC 0179-0126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ethacrynic acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130110
Marketing Category Name NDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name ETHACRYNIC ACID
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of EDECRIN


General Information