Home > National Drug Code (NDC) > Amitriptyline Hydrochloride

Amitriptyline Hydrochloride - 49999-318-30 - (Amitriptyline Hydrochloride)

Alphabetical Index


Drug Information of Amitriptyline Hydrochloride

Product NDC: 49999-318
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: 49999-318
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086009
Marketing Category: ANDA
Start Marketing Date: 20110302

Package Information of Amitriptyline Hydrochloride

Package NDC: 49999-318-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-318-30)

NDC Information of Amitriptyline Hydrochloride

NDC Code 49999-318-30
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-318-30)
Product NDC 49999-318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110302
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


General Information