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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    Pristiq

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    01 3ACTAVIS LABS FL

    02 3ALEMBIC

    03 2ALEMBIC PHARMS LTD

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    05 3HIKMA

    06 2INTELLIPHARMACEUTICS

    07 3LUPIN LTD

    08 2NORVIUM BIOSCIENCE

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    10 3PF PRISM CV

    11 3RUBICON

    12 3YICHANG HUMANWELL

    13 3ZYDUS PHARMS

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    01

    ALEMBIC

    India
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    ALEMBIC

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    RLD : No

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : DESVENLAFAXINE SUCCINATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 50MG BASE

    Approval Date : 2015-06-29

    Application Number : 204003

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    ALEMBIC

    India
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    ALEMBIC

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    RLD : No

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : DESVENLAFAXINE SUCCINATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2015-06-29

    Application Number : 204003

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    ALEMBIC

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    ALEMBIC

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    RLD : No

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : DESVENLAFAXINE SUCCINATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 25MG BASE

    Approval Date : 2018-09-14

    Application Number : 204003

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    ANCHEN PHARMS

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    RLD :

    TE Code :

    DESVENLAFAXINE

    Brand Name : DESVENLAFAXINE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 50MG

    Approval Date :

    Application Number : 204009

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    ANCHEN PHARMS

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    ANCHEN PHARMS

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    RLD :

    TE Code :

    DESVENLAFAXINE

    Brand Name : DESVENLAFAXINE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 100MG

    Approval Date :

    Application Number : 204009

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    PF PRISM CV

    U.S.A
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    RLD : Yes

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : PRISTIQ

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 50MG BASE

    Approval Date : 2008-02-29

    Application Number : 21992

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    PF PRISM CV

    U.S.A
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    PF PRISM CV

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    RLD : Yes

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : PRISTIQ

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2008-02-29

    Application Number : 21992

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    08

    PF PRISM CV

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    PF PRISM CV

    U.S.A
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    Pharma, Lab & Chemical Expo
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    RLD : Yes

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : PRISTIQ

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 25MG BASE

    Approval Date : 2014-08-20

    Application Number : 21992

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    09

    ZYDUS PHARMS

    U.S.A
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    ZYDUS PHARMS

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    RLD : No

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : DESVENLAFAXINE SUCCINATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 50MG BASE

    Approval Date : 2017-10-11

    Application Number : 204020

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    ZYDUS PHARMS

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ZYDUS PHARMS

    U.S.A
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    Pharma, Lab & Chemical Expo
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    RLD : No

    TE Code : AB

    DESVENLAFAXINE SUCCINATE

    Brand Name : DESVENLAFAXINE SUCCINATE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2017-10-11

    Application Number : 204020

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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