Clonidine - 0555-1010-16 - (Clonidine)

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Drug Information of Clonidine

Product NDC: 0555-1010
Proprietary Name: Clonidine
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 Clonidine

Product NDC: 0555-1010
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079090
Marketing Category: ANDA
Start Marketing Date: 20100825

Package Information of Clonidine

Package NDC: 0555-1010-16
Package Description: 4 POUCH in 1 CARTON (0555-1010-16) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH

NDC Information of Clonidine

NDC Code 0555-1010-16
Proprietary Name Clonidine
Package Description 4 POUCH in 1 CARTON (0555-1010-16) > 1 PATCH in 1 POUCH > 24 h in 1 PATCH
Product NDC 0555-1010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine
Dosage Form Name PATCH, EXTENDED RELEASE
Route Name TRANSDERMAL
Start Marketing Date 20100825
Marketing Category Name ANDA
Labeler Name Barr Laboratories 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 Clonidine


General Information