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Protriptyline Hydrochloride - 64980-159-01 - (Protriptyline Hydrochloride)

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Drug Information of Protriptyline Hydrochloride

Product NDC: 64980-159
Proprietary Name: Protriptyline Hydrochloride
Non Proprietary Name: Protriptyline Hydrochloride
Active Ingredient(s): 10    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: 64980-159
Labeler Name: Rising Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090462
Marketing Category: ANDA
Start Marketing Date: 20100611

Package Information of Protriptyline Hydrochloride

Package NDC: 64980-159-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (64980-159-01)

NDC Information of Protriptyline Hydrochloride

NDC Code 64980-159-01
Proprietary Name Protriptyline Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (64980-159-01)
Product NDC 64980-159
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Protriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100611
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals, Inc
Substance Name PROTRIPTYLINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Protriptyline Hydrochloride


General Information