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Nortriptyline Hydrochloride - 63629-2833-6 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 63629-2833
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: 63629-2833
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073554
Marketing Category: ANDA
Start Marketing Date: 19920701

Package Information of Nortriptyline Hydrochloride

Package NDC: 63629-2833-6
Package Description: 50 CAPSULE in 1 BOTTLE (63629-2833-6)

NDC Information of Nortriptyline Hydrochloride

NDC Code 63629-2833-6
Proprietary Name Nortriptyline Hydrochloride
Package Description 50 CAPSULE in 1 BOTTLE (63629-2833-6)
Product NDC 63629-2833
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19920701
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


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