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Nortriptyline Hydrochloride - 0093-0811-01 - (Nortriptyline Hydrochloride)

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Drug Information of Nortriptyline Hydrochloride

Product NDC: 0093-0811
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: 0093-0811
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074132
Marketing Category: ANDA
Start Marketing Date: 19950406

Package Information of Nortriptyline Hydrochloride

Package NDC: 0093-0811-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-0811-01)

NDC Information of Nortriptyline Hydrochloride

NDC Code 0093-0811-01
Proprietary Name Nortriptyline Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0093-0811-01)
Product NDC 0093-0811
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nortriptyline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950406
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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