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Amitriptyline Hydrochloride - 58118-2214-3 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 58118-2214
Proprietary Name: Amitriptyline Hydrochloride
Non Proprietary Name: Amitriptyline Hydrochloride
Active Ingredient(s): 50    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: 58118-2214
Labeler Name: Clinical Solutions Wholesale
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040218
Marketing Category: ANDA
Start Marketing Date: 19970911

Package Information of Amitriptyline Hydrochloride

Package NDC: 58118-2214-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-2214-3)

NDC Information of Amitriptyline Hydrochloride

NDC Code 58118-2214-3
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-2214-3)
Product NDC 58118-2214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970911
Marketing Category Name ANDA
Labeler Name Clinical Solutions Wholesale
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


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