Clonidine - 0378-0872-99 - (clonidine)

Alphabetical Index


Drug Information of Clonidine

Product NDC: 0378-0872
Proprietary Name: Clonidine
Non Proprietary Name: clonidine
Active Ingredient(s): .2    mg/d & nbsp;   clonidine
Administration Route(s): TRANSDERMAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Clonidine

Product NDC: 0378-0872
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076166
Marketing Category: ANDA
Start Marketing Date: 20130208

Package Information of Clonidine

Package NDC: 0378-0872-99
Package Description: 4 POUCH in 1 CARTON (0378-0872-99) > 1 PATCH in 1 POUCH (0378-0872-16) > 7 d in 1 PATCH

NDC Information of Clonidine

NDC Code 0378-0872-99
Proprietary Name Clonidine
Package Description 4 POUCH in 1 CARTON (0378-0872-99) > 1 PATCH in 1 POUCH (0378-0872-16) > 7 d in 1 PATCH
Product NDC 0378-0872
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonidine
Dosage Form Name PATCH
Route Name TRANSDERMAL
Start Marketing Date 20130208
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name CLONIDINE
Strength Number .2
Strength Unit mg/d
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Clonidine


General Information