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Amitriptyline Hydrochloride - 49349-617-02 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 49349-617
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
Coding System: National Drug Codes(NDC)

Labeler Information of Amitriptyline Hydrochloride

Product NDC: 49349-617
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085967
Marketing Category: ANDA
Start Marketing Date: 20111206

Package Information of Amitriptyline Hydrochloride

Package NDC: 49349-617-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-617-02)

NDC Information of Amitriptyline Hydrochloride

NDC Code 49349-617-02
Proprietary Name Amitriptyline Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-617-02)
Product NDC 49349-617
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111206
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name AMITRIPTYLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Amitriptyline Hydrochloride


General Information