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AMITRIPTYLINE HYDROCHLORIDE - 63629-1369-8 - (AMITRIPTYLINE HYDROCHLORIDE)

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Drug Information of AMITRIPTYLINE HYDROCHLORIDE

Product NDC: 63629-1369
Proprietary Name: AMITRIPTYLINE HYDROCHLORIDE
Non Proprietary Name: AMITRIPTYLINE HYDROCHLORIDE
Active Ingredient(s): 25    mg/1 & nbsp;   AMITRIPTYLINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AMITRIPTYLINE HYDROCHLORIDE

Product NDC: 63629-1369
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085966
Marketing Category: ANDA
Start Marketing Date: 20091023

Package Information of AMITRIPTYLINE HYDROCHLORIDE

Package NDC: 63629-1369-8
Package Description: 28 TABLET in 1 BOTTLE (63629-1369-8)

NDC Information of AMITRIPTYLINE HYDROCHLORIDE

NDC Code 63629-1369-8
Proprietary Name AMITRIPTYLINE HYDROCHLORIDE
Package Description 28 TABLET in 1 BOTTLE (63629-1369-8)
Product NDC 63629-1369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMITRIPTYLINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091023
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of AMITRIPTYLINE HYDROCHLORIDE


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