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Amitriptyline Hydrochloride - 51079-147-20 - (amitriptyline hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 51079-147
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: 51079-147
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086009
Marketing Category: ANDA
Start Marketing Date: 20130313

Package Information of Amitriptyline Hydrochloride

Package NDC: 51079-147-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-147-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-147-01)

NDC Information of Amitriptyline Hydrochloride

NDC Code 51079-147-20
Proprietary Name Amitriptyline Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-147-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-147-01)
Product NDC 51079-147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amitriptyline hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130313
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
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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