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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Phentermine Hydrochloride

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    01 1ABC HOLDING

    02 7Actavis Inc

    03 1Aurobindo Pharma Limited

    04 2Aurolife Pharma LLC

    05 1Avanthi Pharma

    06 3Barr Laboratories

    07 2Camall

    08 14Chartwell Pharmaceuticals llc

    09 3Citius Pharmaceuticals

    10 1DURAMED PHARMS BARR

    11 8Elite Laboratories

    12 1Ferndale Laboratories, Inc.

    13 1GSK

    14 1Hanlim Pharmaceuticals Inc

    15 2IVAX Pharmaceuticals Inc

    16 5InvaGen Pharmaceuticals Inc

    17 6KVK.Tech

    18 5Lannett Company, Inc.

    19 3MAST MM

    20 1Merro Pharmaceutical

    21 1Myungmoon Pharm. Co., LTD.

    22 1Novast Laboratories

    23 4Nuvo Pharmaceuticals

    24 1Prinston

    25 1SHIRE PLC

    26 11Sandoz B2B

    27 1Solvay Chemicals International S.A

    28 8Sun Pharmaceutical Industries Limited

    29 1TG United

    30 8Teva Pharmaceutical Industries

    31 4USL PHARMA

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    01

    Actavis Inc

    Ireland
    BioAsia
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    Ireland
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    Regulatory Info : DISCN

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 1998-11-25

    Application Number : 40276

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Chartwell Pharmaceuticals llc

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 8MG

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    Approval Date : 1982-01-01

    Application Number : 83923

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    Registration Country : USA

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    03

    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 1997-05-30

    Application Number : 40190

    Regulatory Info : RX

    Registration Country : USA

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    04

    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 1997-06-18

    Application Number : 40227

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    Registration Country : USA

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    05

    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 1997-06-19

    Application Number : 40228

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    06

    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2003-01-22

    Application Number : 40448

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    07

    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2003-01-14

    Application Number : 40460

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    08

    GSK

    United Kingdom
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    GSK

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : FASTIN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG **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 : 17352

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    KVK.Tech

    U.S.A
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    Regulatory Info : RX

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2008-03-21

    Application Number : 40875

    Regulatory Info : RX

    Registration Country : USA

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    10

    KVK.Tech

    U.S.A
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    Regulatory Info : RX

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 2008-03-31

    Application Number : 40876

    Regulatory Info : RX

    Registration Country : USA

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    11

    KVK.Tech

    U.S.A
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    Regulatory Info : RX

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2008-03-31

    Application Number : 40886

    Regulatory Info : RX

    Registration Country : USA

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    12

    KVK.Tech

    U.S.A
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    KVK.Tech

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    Regulatory Info : RX

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2008-03-31

    Application Number : 40886

    Regulatory Info : RX

    Registration Country : USA

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    13

    KVK.Tech

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2008-04-24

    Application Number : 40887

    Regulatory Info : RX

    Registration Country : USA

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    14

    Lannett Company, Inc.

    U.S.A
    BioAsia
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    U.S.A
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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2005-04-15

    Application Number : 40555

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Prinston

    U.S.A
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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2002-01-04

    Application Number : 40377

    Regulatory Info : RX

    Registration Country : USA

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    16

    Sandoz B2B

    Switzerland
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    Sandoz B2B

    Switzerland
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : WILPO

    Dosage Form : TABLET;ORAL

    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

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Sun Pharmaceutical Industries Limit...

    India
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    Sun Pharmaceutical Industries Limit...

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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 2001-08-30

    Application Number : 40402

    Regulatory Info : DISCN

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2001-08-30

    Application Number : 40403

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sun Pharmaceutical Industries Limit...

    India
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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 : 40427

    Regulatory Info : DISCN

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
    The Generic Rx Session
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    India
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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2003-03-13

    Application Number : 40497

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Sun Pharmaceutical Industries Limit...

    India
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    India
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2003-10-23

    Application Number : 40525

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Sun Pharmaceutical Industries Limit...

    India
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    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2003-10-23

    Application Number : 40526

    Regulatory Info : RX

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
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    Brand Name : PHENTERMINE HYDROCHLORIDE

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    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2003-10-23

    Application Number : 40527

    Regulatory Info : DISCN

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
    The Generic Rx Session
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    Approval Date : 2007-08-21

    Application Number : 40790

    Regulatory Info : DISCN

    Registration Country : USA

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    TG United

    U.S.A
    BioAsia
    Not Confirmed
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    TG United

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 1997-03-07

    Application Number : 40083

    Regulatory Info : DISCN

    Registration Country : USA

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    USL PHARMA

    United Kingdom
    BioAsia
    Not Confirmed
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    USL PHARMA

    United Kingdom
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    BioAsia
    Not Confirmed
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    Regulatory Info : DISCN

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 8MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83804

    Regulatory Info : DISCN

    Registration Country : USA

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    Vivus

    U.S.A
    BioAsia
    Not Confirmed
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    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 3.75MG BASE;23MG

    Packaging :

    Approval Date : 2012-07-17

    Application Number : 22580

    Regulatory Info : RX

    Registration Country : USA

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    28

    Vivus

    U.S.A
    BioAsia
    Not Confirmed
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    Vivus

    U.S.A
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    BioAsia
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    Regulatory Info : RX

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    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 7.5MG BASE;46MG

    Packaging :

    Approval Date : 2012-07-17

    Application Number : 22580

    Regulatory Info : RX

    Registration Country : USA

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    29

    Vivus

    U.S.A
    BioAsia
    Not Confirmed
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    Vivus

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 11.25MG BASE;69MG

    Packaging :

    Approval Date : 2012-07-17

    Application Number : 22580

    Regulatory Info : RX

    Registration Country : USA

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    Vivus

    U.S.A
    BioAsia
    Not Confirmed
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    Vivus

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Brand Name : QSYMIA

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE;92MG

    Packaging :

    Approval Date : 2012-07-17

    Application Number : 22580

    Regulatory Info : RX

    Registration Country : USA

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