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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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    Loxapine Succinate

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    01 4Actavis Inc

    02 4Elite Laboratories

    03 4Lannett Company, Inc.

    04 3PENDOPHARM DIVISION OF DE PHARMASCIENCE INC

    05 4Rising Pharmaceuticals Inc

    06 7Teva Pharmaceutical Industries

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    01

    Actavis Inc

    Ireland
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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 72062

    Regulatory Info : RX

    Registration Country : USA

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    02

    Actavis Inc

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1988-06-15

    Application Number : 72204

    Regulatory Info : RX

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    03

    Actavis Inc

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1988-06-15

    Application Number : 72205

    Regulatory Info : RX

    Registration Country : USA

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    04

    Actavis Inc

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    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 1988-06-15

    Application Number : 72206

    Regulatory Info : RX

    Registration Country : USA

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    05

    Elite Laboratories

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

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    Dosage Strength : EQ 5MG BASE

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    Approval Date : 2005-08-04

    Application Number : 76868

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    Registration Country : USA

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    06

    Elite Laboratories

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    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 2005-08-04

    Application Number : 76868

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    07

    Elite Laboratories

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    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 2005-08-04

    Application Number : 76868

    Regulatory Info : RX

    Registration Country : USA

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    08

    Elite Laboratories

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    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

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    Approval Date : 2005-08-04

    Application Number : 76868

    Regulatory Info : RX

    Registration Country : USA

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    09

    Lannett Company, Inc.

    U.S.A
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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2011-09-26

    Application Number : 90695

    Regulatory Info : RX

    Registration Country : USA

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    10

    Lannett Company, Inc.

    U.S.A
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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 2011-09-26

    Application Number : 90695

    Regulatory Info : RX

    Registration Country : USA

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    11

    Lannett Company, Inc.

    U.S.A
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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2011-09-26

    Application Number : 90695

    Regulatory Info : RX

    Registration Country : USA

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    12

    Lannett Company, Inc.

    U.S.A
    Antibody Engineering
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    Lannett Company, Inc.

    U.S.A
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    Regulatory Info : RX

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 2011-09-26

    Application Number : 90695

    Regulatory Info : RX

    Registration Country : USA

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    13

    PENDOPHARM DIVISION OF DE PHARMASCI...

    Canada
    Antibody Engineering
    Not Confirmed
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    PENDOPHARM DIVISION OF DE PHARMASCI...

    Canada
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    LOXAPINE (LOXAPINE SUCCINATE)

    Brand Name : XYLAC

    Dosage Form : TABLET

    Dosage Strength : 25MG

    Packaging : 100/500

    Approval Date :

    Application Number : 2230839

    Regulatory Info : Prescription

    Registration Country : Canada

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    14

    PENDOPHARM DIVISION OF DE PHARMASCI...

    Canada
    Antibody Engineering
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    Canada
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    LOXAPINE (LOXAPINE SUCCINATE)

    Brand Name : XYLAC

    Dosage Form : TABLET

    Dosage Strength : 10MG

    Packaging : 100

    Approval Date :

    Application Number : 2230838

    Regulatory Info : Prescription

    Registration Country : Canada

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    15

    PENDOPHARM DIVISION OF DE PHARMASCI...

    Canada
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    LOXAPINE (LOXAPINE SUCCINATE)

    Brand Name : XYLAC

    Dosage Form : TABLET

    Dosage Strength : 2.5MG

    Packaging : 100

    Approval Date :

    Application Number : 2242868

    Regulatory Info : Prescription

    Registration Country : Canada

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    16

    Rising Pharmaceuticals Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2004-11-01

    Application Number : 76762

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Rising Pharmaceuticals Inc

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 2004-11-01

    Application Number : 76762

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Rising Pharmaceuticals Inc

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 2004-11-01

    Application Number : 76762

    Regulatory Info : DISCN

    Registration Country : USA

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    Rising Pharmaceuticals Inc

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    LOXAPINE SUCCINATE

    Brand Name : LOXAPINE SUCCINATE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 2004-11-01

    Application Number : 76762

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    Regulatory Info : DISCN

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    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    Regulatory Info : DISCN

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    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was discontinued or withdrawn for s or e reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

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    Portfolio PDF

    Product Web Link

    Virtual Booth

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    Website

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    25

    Teva Pharmaceutical Industries

    Israel
    Antibody Engineering
    Not Confirmed
    arrow

    Teva Pharmaceutical Industries

    Israel
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    26

    Teva Pharmaceutical Industries

    Israel
    Antibody Engineering
    Not Confirmed
    arrow

    Teva Pharmaceutical Industries

    Israel
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag Israel
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    LOXAPINE SUCCINATE

    Brand Name : LOXITANE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 17525

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF