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AMITRIPTYLINE HYDROCHLORIDE - 24236-006-33 - (AMITRIPTYLINE HYDROCHLORIDE)

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Drug Information of AMITRIPTYLINE HYDROCHLORIDE

Product NDC: 24236-006
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
Coding System: National Drug Codes(NDC)

Labeler Information of AMITRIPTYLINE HYDROCHLORIDE

Product NDC: 24236-006
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040218
Marketing Category: ANDA
Start Marketing Date: 20101213

Package Information of AMITRIPTYLINE HYDROCHLORIDE

Package NDC: 24236-006-33
Package Description: 1000 TABLET in 1 CANISTER (24236-006-33)

NDC Information of AMITRIPTYLINE HYDROCHLORIDE

NDC Code 24236-006-33
Proprietary Name AMITRIPTYLINE HYDROCHLORIDE
Package Description 1000 TABLET in 1 CANISTER (24236-006-33)
Product NDC 24236-006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMITRIPTYLINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101213
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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