Home > National Drug Code (NDC) > Clonidine Hydrochloride

Clonidine Hydrochloride - 54868-1967-1 - (Clonidine Hydrochloride)

Alphabetical Index


Drug Information of Clonidine Hydrochloride

Product NDC: 54868-1967
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .3    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: 54868-1967
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070923
Marketing Category: ANDA
Start Marketing Date: 20041130

Package Information of Clonidine Hydrochloride

Package NDC: 54868-1967-1
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (54868-1967-1)

NDC Information of Clonidine Hydrochloride

NDC Code 54868-1967-1
Proprietary Name Clonidine Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (54868-1967-1)
Product NDC 54868-1967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041130
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .3
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Clonidine Hydrochloride


General Information