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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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    Meclofenamic Acid

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    A&M Therapy

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

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    Approval Date : 1987-02-10

    Application Number : 71362

    Regulatory Info : DISCN

    Registration Country : USA

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    A&M Therapy

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 1987-02-10

    Application Number : 71363

    Regulatory Info : DISCN

    Registration Country : USA

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    Actavis Inc

    Ireland
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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

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    Approval Date : 1986-11-25

    Application Number : 70400

    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 1986-11-25

    Application Number : 70401

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    Actavis Inc

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

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    Approval Date : 1987-08-11

    Application Number : 71640

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    Actavis Inc

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 1987-08-11

    Application Number : 71641

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    ANI Pharmaceuticals Inc

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 1987-04-15

    Application Number : 71469

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    Registration Country : USA

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    ANI Pharmaceuticals Inc

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-04-15

    Application Number : 71469

    Regulatory Info : DISCN

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    Barr Laboratories

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1989-03-20

    Application Number : 72809

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Barr Laboratories

    U.S.A
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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1989-03-20

    Application Number : 72848

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Chartwell Pharmaceuticals llc

    U.S.A
    Pharma, Lab & Chemical Expo
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    Chartwell Pharmaceuticals llc

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-11-29

    Application Number : 72262

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Chartwell Pharmaceuticals llc

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-11-29

    Application Number : 72263

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Menarini

    Italy
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Menarini

    Italy
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    Registration Country : Italy

    Meclofenamic Acid

    Brand Name : Lenidolor

    Dosage Form :

    Dosage Strength : 10 Supp 200 Mg  

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    Approval Date :

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    Regulatory Info :

    Registration Country : Italy

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    14

    Menarini

    Italy
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    Meclofenamic Acid

    Brand Name : Lenidolor

    Dosage Form :

    Dosage Strength : 30 Cps 100 Mg  

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    Approval Date :

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    Registration Country : Italy

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    Par Pharmaceutical

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

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    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-03-10

    Application Number : 72077

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Par Pharmaceutical

    U.S.A
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    Not Confirmed
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    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-03-10

    Application Number : 72078

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Pfizer Inc

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

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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOMEN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18006

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Pfizer Inc

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

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    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLOMEN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18006

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    USL PHARMA

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    USL PHARMA

    United Kingdom
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-03-25

    Application Number : 71007

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    USL PHARMA

    United Kingdom
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    USL PHARMA

    United Kingdom
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-03-25

    Application Number : 71008

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Viatris

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

    U.S.A
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    Pharma, Lab & Chemical Expo
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    Regulatory Info : RX

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1986-09-03

    Application Number : 71081

    Regulatory Info : RX

    Registration Country : USA

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    22

    Viatris

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

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1986-09-03

    Application Number : 71081

    Regulatory Info : RX

    Registration Country : USA

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    23

    QUANTUM PHARMICS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    QUANTUM PHARMICS

    Country
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    Regulatory Info : DISCN

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    MECLOFENAMATE SODIUM

    Brand Name : MECLODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-07-14

    Application Number : 71380

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    QUANTUM PHARMICS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    QUANTUM PHARMICS

    Country
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1987-07-14

    Application Number : 71381

    Regulatory Info : DISCN

    Registration Country : USA

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    VITARINE

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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    VITARINE

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    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 71684

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    VITARINE

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    Not Confirmed
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    VITARINE

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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 71710

    Regulatory Info : DISCN

    Registration Country : USA

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    PHARMAFAR Srl

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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    PHARMAFAR Srl

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    Regulatory Info :

    Registration Country : Italy

    Meclofenamic Acid

    Brand Name : Movens

    Dosage Form :

    Dosage Strength : 30 Cps 100 Mg  

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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