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Amitriptyline Hydrochloride - 67046-015-30 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 67046-015
Proprietary Name: Amitriptyline Hydrochloride
Non Proprietary Name: Amitriptyline Hydrochloride
Active Ingredient(s): 100    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: 67046-015
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085967
Marketing Category: ANDA
Start Marketing Date: 20100216

Package Information of Amitriptyline Hydrochloride

Package NDC: 67046-015-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-015-30)

NDC Information of Amitriptyline Hydrochloride

NDC Code 67046-015-30
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-015-30)
Product NDC 67046-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100216
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


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