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Nortriptyline Hydrochloride - 54868-2480-0 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 54868-2480
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: 54868-2480
Labeler Name: Physicians Total Care, inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073556
Marketing Category: ANDA
Start Marketing Date: 19930910

Package Information of Nortriptyline Hydrochloride

Package NDC: 54868-2480-0
Package Description: 100 CAPSULE in 1 BOTTLE (54868-2480-0)

NDC Information of Nortriptyline Hydrochloride

NDC Code 54868-2480-0
Proprietary Name Nortriptyline Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (54868-2480-0)
Product NDC 54868-2480
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19930910
Marketing Category Name ANDA
Labeler Name Physicians Total Care, inc.
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


General Information