DARANIDE - 51672-4144-0 - (dichlorphenamide)

Alphabetical Index


Drug Information of DARANIDE

Product NDC: 51672-4144
Proprietary Name: DARANIDE
Non Proprietary Name: dichlorphenamide
Active Ingredient(s): 50    mg/1 & nbsp;   dichlorphenamide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DARANIDE

Product NDC: 51672-4144
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011366
Marketing Category: NDA
Start Marketing Date: 20120316

Package Information of DARANIDE

Package NDC: 51672-4144-0
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51672-4144-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of DARANIDE

NDC Code 51672-4144-0
Proprietary Name DARANIDE
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51672-4144-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 51672-4144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dichlorphenamide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120316
Marketing Category Name NDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name DICHLORPHENAMIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of DARANIDE


General Information