Home > National Drug Code (NDC) > Nortriptyline Hydrochloride

Nortriptyline Hydrochloride - 67544-078-60 - (Nortriptyline Hydrochloride)

Alphabetical Index


Drug Information of Nortriptyline Hydrochloride

Product NDC: 67544-078
Proprietary Name: Nortriptyline Hydrochloride
Non Proprietary Name: Nortriptyline Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Nortriptyline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nortriptyline Hydrochloride

Product NDC: 67544-078
Labeler Name: Aphena Pharma Solutions - Tennessee, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074132
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Nortriptyline Hydrochloride

Package NDC: 67544-078-60
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (67544-078-60)

NDC Information of Nortriptyline Hydrochloride

NDC Code 67544-078-60
Proprietary Name Nortriptyline Hydrochloride
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (67544-078-60)
Product NDC 67544-078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110531
Marketing Category Name ANDA
Labeler Name Aphena Pharma Solutions - Tennessee, Inc.
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


General Information