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Nortriptyline Hydrochloride - 68084-031-01 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 68084-031
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: 68084-031
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073553
Marketing Category: ANDA
Start Marketing Date: 20110519

Package Information of Nortriptyline Hydrochloride

Package NDC: 68084-031-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-031-01) > 10 CAPSULE in 1 BLISTER PACK (68084-031-11)

NDC Information of Nortriptyline Hydrochloride

NDC Code 68084-031-01
Proprietary Name Nortriptyline Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-031-01) > 10 CAPSULE in 1 BLISTER PACK (68084-031-11)
Product NDC 68084-031
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 American Health Packaging
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


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