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Last Updated: November 21, 2024

DESVENLAFAXINE Drug Patent Profile


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Which patents cover Desvenlafaxine, and what generic alternatives are available?

Desvenlafaxine is a drug marketed by Alembic Pharms Ltd, Sun Pharm, Teva Pharms Usa, Actavis Labs Fl, Alembic, Hikma, Intellipharmaceutics, Lupin Ltd, Norvium Bioscience, Rubicon, Yichang Humanwell, and Zydus Pharms. and is included in thirteen NDAs.

The generic ingredient in DESVENLAFAXINE is desvenlafaxine succinate. There are sixteen drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the desvenlafaxine succinate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Desvenlafaxine

A generic version of DESVENLAFAXINE was approved as desvenlafaxine succinate by ALEMBIC on June 29th, 2015.

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Summary for DESVENLAFAXINE
Drug patent expirations by year for DESVENLAFAXINE
Drug Prices for DESVENLAFAXINE

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Recent Clinical Trials for DESVENLAFAXINE

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da SaudePhase 2
Sage TherapeuticsPhase 3
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.Phase 3

See all DESVENLAFAXINE clinical trials

Anatomical Therapeutic Chemical (ATC) Classes for DESVENLAFAXINE

US Patents and Regulatory Information for DESVENLAFAXINE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Yichang Humanwell DESVENLAFAXINE SUCCINATE desvenlafaxine succinate TABLET, EXTENDED RELEASE;ORAL 210014-002 Oct 1, 2018 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Zydus Pharms DESVENLAFAXINE SUCCINATE desvenlafaxine succinate TABLET, EXTENDED RELEASE;ORAL 204020-003 Nov 30, 2022 AB RX No No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Alembic Pharms Ltd DESVENLAFAXINE desvenlafaxine TABLET, EXTENDED RELEASE;ORAL 204150-001 Mar 4, 2013 RX Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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