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Nortriptyline Hydrochloride - 49999-915-60 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 49999-915
Proprietary Name: Nortriptyline Hydrochloride
Non Proprietary Name: Nortriptyline Hydrochloride
Active Ingredient(s): 50    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: 49999-915
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073555
Marketing Category: ANDA
Start Marketing Date: 20111205

Package Information of Nortriptyline Hydrochloride

Package NDC: 49999-915-60
Package Description: 60 CAPSULE in 1 BOTTLE (49999-915-60)

NDC Information of Nortriptyline Hydrochloride

NDC Code 49999-915-60
Proprietary Name Nortriptyline Hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (49999-915-60)
Product NDC 49999-915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111205
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name NORTRIPTYLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Nortriptyline Hydrochloride


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