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Amitriptyline Hydrochloride - 49999-063-90 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 49999-063
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amitriptyline Hydrochloride

Product NDC: 49999-063
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085966
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Amitriptyline Hydrochloride

Package NDC: 49999-063-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-063-90)

NDC Information of Amitriptyline Hydrochloride

NDC Code 49999-063-90
Proprietary Name Amitriptyline Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-063-90)
Product NDC 49999-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110531
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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