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    04 1AAIPharma Services Corp.

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    LGM Pharma

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    Virtual BoothLGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    Approval Date : 2019-08-30

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    Aspen Pharmacare Holdings

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    LGM Pharma

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    NABUMETONE

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    Approval Date : 2019-08-30

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    LGM Pharma

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    NABUMETONE

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    Approval Date : 2019-08-30

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    Aspen Pharmacare Holdings

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    Chartwell Pharmaceuticals llc

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    Approval Date : 2002-02-25

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    Chartwell Pharmaceuticals llc

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    08

    Chartwell Pharmaceuticals llc

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    Chartwell Pharmaceuticals llc

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    NABUMETONE

    Brand Name : NABUMETONE

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    Approval Date : 2003-01-24

    Application Number : 76009

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    09

    Chartwell Pharmaceuticals llc

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    Brand Name : NABUMETONE

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    Approval Date : 2003-01-24

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    Copley Scientific

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    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 750MG

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    Approval Date : 2000-06-06

    Application Number : 75179

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    11

    Epic Pharma. LLC.

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    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2002-02-25

    Application Number : 75590

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    12

    Epic Pharma. LLC.

    U.S.A
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    Regulatory Info : DISCN

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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 750MG

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    Approval Date : 2002-02-25

    Application Number : 75590

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    GSK

    United Kingdom
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    GSK

    United Kingdom
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    NABUMETONE

    Brand Name : RELAFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-12-24

    Application Number : 19583

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    GSK

    United Kingdom
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

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    NABUMETONE

    Brand Name : RELAFEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-12-24

    Application Number : 19583

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Impax Laboratories

    U.S.A
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    Impax Laboratories

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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

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    Approval Date : 2000-05-26

    Application Number : 75189

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Impax Laboratories

    U.S.A
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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 750MG

    Packaging :

    Approval Date : 2001-09-24

    Application Number : 75189

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    InvaGen Pharmaceuticals Inc

    U.S.A
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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

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    Approval Date : 2008-03-07

    Application Number : 78671

    Regulatory Info : RX

    Registration Country : USA

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    18

    InvaGen Pharmaceuticals Inc

    U.S.A
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    InvaGen Pharmaceuticals Inc

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    Brand Name : NABUMETONE

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    Approval Date : 2008-03-07

    Application Number : 78671

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    19

    ScieGen Pharmaceuticals

    U.S.A
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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2008-09-24

    Application Number : 78420

    Regulatory Info : RX

    Registration Country : USA

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    ScieGen Pharmaceuticals

    U.S.A
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    NABUMETONE

    Brand Name : NABUMETONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 750MG

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    Approval Date : 2008-09-24

    Application Number : 78420

    Regulatory Info : RX

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.