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Amitriptyline Hydrochloride - 21695-252-30 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 21695-252
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: 21695-252
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085968
Marketing Category: ANDA
Start Marketing Date: 19771129

Package Information of Amitriptyline Hydrochloride

Package NDC: 21695-252-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-252-30)

NDC Information of Amitriptyline Hydrochloride

NDC Code 21695-252-30
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-252-30)
Product NDC 21695-252
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 Rebel Distributors Corp.
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


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