Catapres - 0597-0032-34 - (clonidine)

Alphabetical Index


Drug Information of Catapres

Product NDC: 0597-0032
Proprietary Name: Catapres
Non Proprietary Name: clonidine
Active Ingredient(s): .2    mg/24h & nbsp;   clonidine
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Catapres

Product NDC: 0597-0032
Labeler Name: Boehringer Ingelheim Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018891
Marketing Category: NDA
Start Marketing Date: 19851001

Package Information of Catapres

Package NDC: 0597-0032-34
Package Description: 4 POUCH in 1 CARTON (0597-0032-34) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH

NDC Information of Catapres

NDC Code 0597-0032-34
Proprietary Name Catapres
Package Description 4 POUCH in 1 CARTON (0597-0032-34) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH
Product NDC 0597-0032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonidine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 19851001
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals Inc.
Substance Name CLONIDINE
Strength Number .2
Strength Unit mg/24h
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Catapres


General Information