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    Dr. Reddy's Laboratories

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    Actavis Inc

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    Approval Date : 1998-11-25

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    Approval Date : 1997-06-18

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    Approval Date : 1997-06-19

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    Elite Laboratories

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    PHENTERMINE HYDROCHLORIDE

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    Approval Date : 1982-01-01

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    Approval Date : 2002-01-04

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    Sandoz B2B

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    Brand Name : WILPO

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    Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 12737

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    13

    Sun Pharmaceutical Industries Limit...

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    Approval Date : 2001-08-30

    Application Number : 40402

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    Sun Pharmaceutical Industries Limit...

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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2001-08-30

    Application Number : 40403

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    Sun Pharmaceutical Industries Limit...

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    Approval Date : 2001-08-30

    Application Number : 40427

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    TG United

    U.S.A
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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 1997-03-07

    Application Number : 40083

    Regulatory Info : DISCN

    Registration Country : USA

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    Vivus

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    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 3.75MG BASE;23MG

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    Approval Date : 2012-07-17

    Application Number : 22580

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    Vivus

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    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 7.5MG BASE;46MG

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    Approval Date : 2012-07-17

    Application Number : 22580

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    Vivus

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    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 11.25MG BASE;69MG

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    Approval Date : 2012-07-17

    Application Number : 22580

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    Registration Country : USA

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    Vivus

    U.S.A
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    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE;92MG

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    Approval Date : 2012-07-17

    Application Number : 22580

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