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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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    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 2Pharma Dynamics

    25 1Prinston

    26 1SHIRE PLC

    27 11Sandoz B2B

    28 1Solvay Chemicals International S.A

    29 8Sun Pharmaceutical Industries Limited

    30 1TG United

    31 8Teva Pharmaceutical Industries

    32 4USL PHARMA

    33 2Upsher-Smith Laboratories

    34 4VITARINE

    35 4Vivus

    36 3Zydus Pharmaceuticals

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    01

    Actavis Inc

    Ireland
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    Actavis Inc

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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 : 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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    Chartwell Pharmaceuticals llc

    U.S.A
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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 : 83923

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Elite Laboratories

    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 : 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

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Elite Laboratories

    U.S.A
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    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

    Regulatory Info : RX

    Registration Country : USA

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    06

    Elite Laboratories

    U.S.A
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    Elite Laboratories

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2003-01-22

    Application Number : 40448

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Elite Laboratories

    U.S.A
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    Elite Laboratories

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2003-01-14

    Application Number : 40460

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    GSK

    United Kingdom
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    GSK

    United Kingdom
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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**

    Packaging :

    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

    Registration Country : USA

    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    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

    Packaging :

    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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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    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

    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 : 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
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    Lannett Company, Inc.

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    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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    Prinston

    U.S.A
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    PHENTERMINE HYDROCHLORIDE

    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**

    Packaging :

    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...

    India
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

    Packaging :

    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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    Sun Pharmaceutical Industries Limit...

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2001-08-30

    Application Number : 40403

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Sun Pharmaceutical Industries Limit...

    India
    Antibody Engineering
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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

    Packaging :

    Approval Date : 2001-08-30

    Application Number : 40427

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Sun Pharmaceutical Industries Limit...

    India
    Antibody Engineering
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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 : 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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    Sun Pharmaceutical Industries Limit...

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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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    Sun Pharmaceutical Industries Limit...

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    PHENTERMINE HYDROCHLORIDE

    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...

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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 2003-10-23

    Application Number : 40527

    Regulatory Info : DISCN

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
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    Sun Pharmaceutical Industries Limit...

    India
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    PHENTERMINE HYDROCHLORIDE

    Brand Name : PHENTERMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 37.5MG

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    Approval Date : 2007-08-21

    Application Number : 40790

    Regulatory Info : DISCN

    Registration Country : USA

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    TG United

    U.S.A
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    Regulatory Info : DISCN

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    PHENTERMINE HYDROCHLORIDE

    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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    USL PHARMA

    United Kingdom
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    United Kingdom
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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
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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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    Vivus

    U.S.A
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    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    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

    Regulatory Info : RX

    Registration Country : USA

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    Vivus

    U.S.A
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    Vivus

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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 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
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    Vivus

    U.S.A
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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 15MG BASE;92MG

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    Approval Date : 2012-07-17

    Application Number : 22580

    Regulatory Info : RX

    Registration Country : USA

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