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Amitriptyline Hydrochloride - 60760-214-10 - (Amitriptyline Hydrochloride)

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Drug Information of Amitriptyline Hydrochloride

Product NDC: 60760-214
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
Coding System: National Drug Codes(NDC)

Labeler Information of Amitriptyline Hydrochloride

Product NDC: 60760-214
Labeler Name: St. Mary's Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040218
Marketing Category: ANDA
Start Marketing Date: 20091201

Package Information of Amitriptyline Hydrochloride

Package NDC: 60760-214-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (60760-214-10)

NDC Information of Amitriptyline Hydrochloride

NDC Code 60760-214-10
Proprietary Name Amitriptyline Hydrochloride
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (60760-214-10)
Product NDC 60760-214
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amitriptyline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091201
Marketing Category Name ANDA
Labeler Name St. Mary's Medical Park Pharmacy
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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