Home > National Drug Code (NDC) > Amitriptyline Hydrochloride

Amitriptyline Hydrochloride - 35356-742-60 - (Amitriptyline Hydrochloride)

Alphabetical Index


Drug Information of Amitriptyline Hydrochloride

Product NDC: 35356-742
Proprietary Name: Amitriptyline Hydrochloride
Non Proprietary Name: Amitriptyline Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Amitriptyline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amitriptyline Hydrochloride

Product NDC: 35356-742
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085968
Marketing Category: ANDA
Start Marketing Date: 19771129

Package Information of Amitriptyline Hydrochloride

Package NDC: 35356-742-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (35356-742-60)

NDC Information of Amitriptyline Hydrochloride

NDC Code 35356-742-60
Proprietary Name Amitriptyline Hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (35356-742-60)
Product NDC 35356-742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19771129
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


General Information