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Nortriptyline Hydrochloride - 55289-099-50 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 55289-099
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: 55289-099
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073554
Marketing Category: ANDA
Start Marketing Date: 19920701

Package Information of Nortriptyline Hydrochloride

Package NDC: 55289-099-50
Package Description: 50 CAPSULE in 1 BOTTLE, PLASTIC (55289-099-50)

NDC Information of Nortriptyline Hydrochloride

NDC Code 55289-099-50
Proprietary Name Nortriptyline Hydrochloride
Package Description 50 CAPSULE in 1 BOTTLE, PLASTIC (55289-099-50)
Product NDC 55289-099
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 PD-Rx Pharmaceuticals, Inc.
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


General Information