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Amitriptyline Hydrochloride - 35356-743-00 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 35356-743
Proprietary Name: Amitriptyline Hydrochloride
Non Proprietary Name: Amitriptyline Hydrochloride
Active Ingredient(s): 100    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: 35356-743
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085967
Marketing Category: ANDA
Start Marketing Date: 19771121

Package Information of Amitriptyline Hydrochloride

Package NDC: 35356-743-00
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (35356-743-00)

NDC Information of Amitriptyline Hydrochloride

NDC Code 35356-743-00
Proprietary Name Amitriptyline Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (35356-743-00)
Product NDC 35356-743
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19771121
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


General Information