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Guanfacine Hydrochloride - 65162-713-03 - (Guanfacine Hydrochloride)

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Drug Information of Guanfacine Hydrochloride

Product NDC: 65162-713
Proprietary Name: Guanfacine Hydrochloride
Non Proprietary Name: Guanfacine Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Guanfacine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Guanfacine Hydrochloride

Product NDC: 65162-713
Labeler Name: Amneal Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075109
Marketing Category: ANDA
Start Marketing Date: 19981125

Package Information of Guanfacine Hydrochloride

Package NDC: 65162-713-03
Package Description: 30 TABLET in 1 BOTTLE (65162-713-03)

NDC Information of Guanfacine Hydrochloride

NDC Code 65162-713-03
Proprietary Name Guanfacine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (65162-713-03)
Product NDC 65162-713
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Guanfacine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981125
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals
Substance Name GUANFACINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Guanfacine Hydrochloride


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