Home > National Drug Code (NDC) > Clonidine Hydrochloride

Clonidine Hydrochloride - 24236-166-33 - (Clonidine Hydrochloride)

Alphabetical Index


Drug Information of Clonidine Hydrochloride

Product NDC: 24236-166
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .1    mg/1 & nbsp;   Clonidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonidine Hydrochloride

Product NDC: 24236-166
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071783
Marketing Category: ANDA
Start Marketing Date: 20110404

Package Information of Clonidine Hydrochloride

Package NDC: 24236-166-33
Package Description: 1000 TABLET in 1 CANISTER (24236-166-33)

NDC Information of Clonidine Hydrochloride

NDC Code 24236-166-33
Proprietary Name Clonidine Hydrochloride
Package Description 1000 TABLET in 1 CANISTER (24236-166-33)
Product NDC 24236-166
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110404
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Clonidine Hydrochloride


General Information