EDECRIN - 25010-205-15 - (ethacrynic acid)

Alphabetical Index


Drug Information of EDECRIN

Product NDC: 25010-205
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: 25010-205
Labeler Name: Aton Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016092
Marketing Category: NDA
Start Marketing Date: 19670110

Package Information of EDECRIN

Package NDC: 25010-205-15
Package Description: 1 BOTTLE in 1 CARTON (25010-205-15) > 100 TABLET in 1 BOTTLE

NDC Information of EDECRIN

NDC Code 25010-205-15
Proprietary Name EDECRIN
Package Description 1 BOTTLE in 1 CARTON (25010-205-15) > 100 TABLET in 1 BOTTLE
Product NDC 25010-205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ethacrynic acid
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19670110
Marketing Category Name NDA
Labeler Name Aton Pharma, Inc.
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