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Nortriptyline Hydrochloride - 68788-9749-6 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 68788-9749
Proprietary Name: Nortriptyline Hydrochloride
Non Proprietary Name: Nortriptyline Hydrochloride
Active Ingredient(s): 10    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: 68788-9749
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074132
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Nortriptyline Hydrochloride

Package NDC: 68788-9749-6
Package Description: 60 CAPSULE in 1 BOTTLE (68788-9749-6)

NDC Information of Nortriptyline Hydrochloride

NDC Code 68788-9749-6
Proprietary Name Nortriptyline Hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (68788-9749-6)
Product NDC 68788-9749
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


General Information