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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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    Cyclobenzaprine Hydrochloride

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    01 2ANDA Repository

    02 1ANGITA PHARMA INC.

    03 5Actavis Inc

    04 2Adcock Ingram

    05 2AiPing Pharmaceutical Inc

    06 3Apotex Inc

    07 2Aspire Lifesciences Pvt Ltd

    08 1Auro Pharma Inc

    09 4Aurobindo Pharma Limited

    10 3Chartwell Pharmaceuticals llc

    11 2Eurofarma Laboratorios S.A

    12 3Graviti Pharmaceuticals

    13 1Grupo Azevedos

    14 2InvaGen Pharmaceuticals Inc

    15 3Inventia Healthcare Limited

    16 1JAMP PHARMA

    17 2Johnson & Johnson Innovative Medicine

    18 3Jubilant Cadista Pharmaceuticals

    19 2KVK.Tech

    20 1LABORATOIRE RIVA INC.

    21 2Macleods Pharmaceuticals Limited

    22 2Novast Laboratories

    23 2Oxford Pharm

    24 1PRO DOC LIMITEE

    25 2Par Pharmaceutical

    26 2Pharmascience Inc.

    27 1Pliva Hrvatska

    28 2Prinston

    29 3Rising Pharmaceuticals Inc

    30 3Rubicon Research

    31 1SANIS HEALTH INC

    32 1SIT LABORATORIO FARMAC. Srl

    33 1SIVEM PHARMACEUTICALS ULC

    34 1Sandoz B2B

    35 2Sudarshan Pharma

    36 3Sun Pharmaceutical Industries Limited

    37 2TWi Pharmaceuticals

    38 3Teva Pharmaceutical Industries

    39 3Unichem Pharmaceuticals USA, Inc

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    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1989-05-03

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    Dosage Form : TABLET;ORAL

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    Approval Date : 2006-02-03

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    Approval Date : 1991-11-27

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1994-11-30

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    AiPing Pharmaceutical Inc

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 1991-11-19

    Application Number : 72854

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2006-02-03

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1995-05-23

    Application Number : 73541

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2006-04-06

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    Chartwell Pharmaceuticals llc

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2008-04-18

    Application Number : 78218

    Regulatory Info : RX

    Registration Country : USA

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    Chartwell Pharmaceuticals llc

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2015-06-19

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    Chartwell Pharmaceuticals llc

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2020-11-03

    Application Number : 78218

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    Johnson & Johnson Innovative Medici...

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    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : FLEXERIL

    Dosage Form : TABLET;ORAL

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

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    Approval Date : 1982-01-01

    Application Number : 17821

    Regulatory Info : DISCN

    Registration Country : USA

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    Brand Name : FLEXERIL

    Dosage Form : TABLET;ORAL

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

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    Approval Date : 1982-01-01

    Application Number : 17821

    Regulatory Info : DISCN

    Registration Country : USA

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    Jubilant Cadista Pharmaceuticals

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2006-04-19

    Application Number : 77563

    Regulatory Info : RX

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    Jubilant Cadista Pharmaceuticals

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2006-04-19

    Application Number : 77563

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    Jubilant Cadista Pharmaceuticals

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2017-08-25

    Application Number : 77563

    Regulatory Info : RX

    Registration Country : USA

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    KVK.Tech

    U.S.A
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    KVK.Tech

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2011-02-28

    Application Number : 78048

    Regulatory Info : RX

    Registration Country : USA

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    KVK.Tech

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    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2011-02-28

    Application Number : 78048

    Regulatory Info : RX

    Registration Country : USA

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    Oxford Pharm

    U.S.A
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    Oxford Pharm

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    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2005-10-04

    Application Number : 77209

    Regulatory Info : RX

    Registration Country : USA

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    Oxford Pharm

    U.S.A
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    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2006-02-03

    Application Number : 77209

    Regulatory Info : RX

    Registration Country : USA

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    Pliva Hrvatska

    Croatia
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    Pliva Hrvatska

    Croatia
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    Virtual Booth Virtual Booth
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    Regulatory Info : DISCN

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1995-09-29

    Application Number : 74421

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    Prinston

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

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2007-02-28

    Application Number : 77797

    Regulatory Info : RX

    Registration Country : USA

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    24

    Prinston

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

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2007-02-28

    Application Number : 77797

    Regulatory Info : RX

    Registration Country : USA

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    25

    Rising Pharmaceuticals Inc

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1991-05-30

    Application Number : 73144

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    Rising Pharmaceuticals Inc

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2006-02-03

    Application Number : 73144

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Rising Pharmaceuticals Inc

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Rising Pharmaceuticals Inc

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2013-03-25

    Application Number : 73144

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Sandoz B2B

    Switzerland
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1993-02-26

    Application Number : 73683

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Teva Pharmaceutical Industries

    Israel
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : AMRIX

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2007-02-01

    Application Number : 21777

    Regulatory Info : RX

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Teva Pharmaceutical Industries

    Israel
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    CYCLOBENZAPRINE HYDROCHLORIDE

    Brand Name : AMRIX

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2007-02-01

    Application Number : 21777

    Regulatory Info : RX

    Registration Country : USA

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