CLONIDINE - 16590-266-71 - (CLONIDINE HCL)

Alphabetical Index


Drug Information of CLONIDINE

Product NDC: 16590-266
Proprietary Name: CLONIDINE
Non Proprietary Name: CLONIDINE HCL
Active Ingredient(s): .1    mg/1 & nbsp;   CLONIDINE HCL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CLONIDINE

Product NDC: 16590-266
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 19861216

Package Information of CLONIDINE

Package NDC: 16590-266-71
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (16590-266-71)

NDC Information of CLONIDINE

NDC Code 16590-266-71
Proprietary Name CLONIDINE
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (16590-266-71)
Product NDC 16590-266
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CLONIDINE HCL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19861216
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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


General Information