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Amitriptyline Hydrochloride - 63629-3597-1 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 63629-3597
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: 63629-3597
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085971
Marketing Category: ANDA
Start Marketing Date: 19771129

Package Information of Amitriptyline Hydrochloride

Package NDC: 63629-3597-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-3597-1)

NDC Information of Amitriptyline Hydrochloride

NDC Code 63629-3597-1
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-3597-1)
Product NDC 63629-3597
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 Bryant Ranch Prepack
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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