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Amitriptyline Hydrochloride - 55154-5665-0 - (amitriptyline hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 55154-5665
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amitriptyline Hydrochloride

Product NDC: 55154-5665
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086009
Marketing Category: ANDA
Start Marketing Date: 20110617

Package Information of Amitriptyline Hydrochloride

Package NDC: 55154-5665-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5665-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Amitriptyline Hydrochloride

NDC Code 55154-5665-0
Proprietary Name Amitriptyline Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5665-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5665
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amitriptyline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110617
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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