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Nortriptyline Hydrochloride - 55154-4774-0 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 55154-4774
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: 55154-4774
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073554
Marketing Category: ANDA
Start Marketing Date: 20110519

Package Information of Nortriptyline Hydrochloride

Package NDC: 55154-4774-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4774-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Nortriptyline Hydrochloride

NDC Code 55154-4774-0
Proprietary Name Nortriptyline Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-4774-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-4774
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110519
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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