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Serving leading biopharmaceutical companies globally:

Cipla
Covington
Healthtrust
Farmers Insurance
Medtronic
US Army
AstraZeneca
Johnson and Johnson
Merck
Moodys

Generated: February 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 078932

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NDA 078932 describes VENLAFAXINE HYDROCHLORIDE, which is a drug marketed by Anchen Pharms, Aurobindo Pharma Ltd, Dr Reddys Labs Ltd, Macleods Pharms Ltd, Mylan, Orchid Hlthcare, Teva, Torrent Pharms Llc, Valeant Pharms North, Wockhardt, Zydus Pharms Usa Inc, Nostrum Labs Inc, Osmotica Pharm, Sun Pharma Global, Alembic Pharms Ltd, Amneal Pharms, Aurobindo Pharma, Fosun Pharma, Heritage Pharms Inc, Pliva Hrvatska Doo, Prinston Inc, Sun Pharm Inds Inc, Yaopharma Co Ltd, and Zydus Pharms Usa, and is included in twenty-seven NDAs. It is available from seventy-one suppliers. Additional details are available on the VENLAFAXINE HYDROCHLORIDE profile page.

The generic ingredient in VENLAFAXINE HYDROCHLORIDE is venlafaxine hydrochloride. There are seventy-one drug master file entries for this compound. Seventy-five suppliers are listed for this compound. Additional details are available on the venlafaxine hydrochloride profile page.
Summary for 078932
Tradename:VENLAFAXINE HYDROCHLORIDE
Applicant:Alembic Pharms Ltd
Ingredient:venlafaxine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details
Pharmacology for NDA: 078932
Suppliers and Packaging for NDA: 078932
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VENLAFAXINE HYDROCHLORIDE venlafaxine hydrochloride TABLET;ORAL 078932 ANDA NorthStar RxLLC 16714-311 N 16714-311-02
VENLAFAXINE HYDROCHLORIDE venlafaxine hydrochloride TABLET;ORAL 078932 ANDA NorthStar RxLLC 16714-311 N 16714-311-03

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 25MG BASE
Approval Date:Dec 14, 2010TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 37.5MG BASE
Approval Date:Dec 14, 2010TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrengthEQ 50MG BASE
Approval Date:Dec 14, 2010TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Harvard Business School
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Baxter
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Chubb
Cantor Fitzgerald
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Julphar
Fuji

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