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Protriptyline Hydrochloride - 42806-096-10 - (Protriptyline Hydrochloride)

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Drug Information of Protriptyline Hydrochloride

Product NDC: 42806-096
Proprietary Name: Protriptyline Hydrochloride
Non Proprietary Name: Protriptyline Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Protriptyline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Protriptyline Hydrochloride

Product NDC: 42806-096
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202220
Marketing Category: ANDA
Start Marketing Date: 20130109

Package Information of Protriptyline Hydrochloride

Package NDC: 42806-096-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (42806-096-10)

NDC Information of Protriptyline Hydrochloride

NDC Code 42806-096-10
Proprietary Name Protriptyline Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (42806-096-10)
Product NDC 42806-096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Protriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130109
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
Substance Name PROTRIPTYLINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Protriptyline Hydrochloride


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