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Serving leading biopharmaceutical companies globally:

Moodys
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Chinese Patent Office
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Dow
Johnson and Johnson
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Generated: December 17, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 014684

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NDA 014684 describes AVENTYL HYDROCHLORIDE, which is a drug marketed by Lilly and is included in one NDA. Additional details are available on the AVENTYL HYDROCHLORIDE profile page.

The generic ingredient in AVENTYL HYDROCHLORIDE is nortriptyline hydrochloride. There are eleven drug master file entries for this compound. Thirty-four suppliers are listed for this compound. Additional details are available on the nortriptyline hydrochloride profile page.

Summary for 014684

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details

Medical Subject Heading (MeSH) Categories for 014684

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 10MG BASE
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Summary for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 25MG BASE
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Expired Orange Book Patents for NDA: 014684

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
LillyAVENTYL HYDROCHLORIDEnortriptyline hydrochlorideCAPSULE;ORAL014684-001Approved Prior to Jan 1, 1982► Subscribe► Subscribe
LillyAVENTYL HYDROCHLORIDEnortriptyline hydrochlorideCAPSULE;ORAL014684-002Approved Prior to Jan 1, 1982► Subscribe► Subscribe
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Serving leading biopharmaceutical companies globally:

Argus Health
AstraZeneca
Julphar
Johnson and Johnson
Moodys
Citi
Express Scripts
Medtronic
Daiichi Sankyo
Harvard Business School

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