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Amitriptyline Hydrochloride - 54868-2357-0 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 54868-2357
Proprietary Name: Amitriptyline Hydrochloride
Non Proprietary Name: Amitriptyline Hydrochloride
Active Ingredient(s): 75    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: 54868-2357
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085971
Marketing Category: ANDA
Start Marketing Date: 20030204

Package Information of Amitriptyline Hydrochloride

Package NDC: 54868-2357-0
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2357-0)

NDC Information of Amitriptyline Hydrochloride

NDC Code 54868-2357-0
Proprietary Name Amitriptyline Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2357-0)
Product NDC 54868-2357
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030204
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


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