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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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    Nadolol

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    01 2Biophore India Pharmaceuticals Pvt Ltd

    02 3Alembic Pharmaceuticals Limited

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    07 3Beximco Pharmaceuticals

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    15 3Novast Laboratories

    16 2Pfizer Inc

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    Biophore India Pharmaceuticals Pvt ...

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    Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Biophore India Pharmaceuticals Pvt ...

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    Virtual BoothBiophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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    Aurobindo Pharma Limited

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

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    Approval Date : 2015-09-16

    Application Number : 201893

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    Aurobindo Pharma Limited

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    Approval Date : 2015-09-16

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    Aurobindo Pharma Limited

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    NADOLOL

    Brand Name : NADOLOL

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    Approval Date : 2022-06-07

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    Avet Pharmaceuticals

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

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    Approval Date : 1996-08-30

    Application Number : 74229

    Regulatory Info : DISCN

    Registration Country : USA

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    Avet Pharmaceuticals

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 1996-08-30

    Application Number : 74229

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    Avet Pharmaceuticals

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

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    Approval Date : 1996-01-24

    Application Number : 74255

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    09

    Avet Pharmaceuticals

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 120MG

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    Approval Date : 1996-01-24

    Application Number : 74255

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    10

    Avet Pharmaceuticals

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    Avet Pharmaceuticals

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 160MG

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    Approval Date : 1996-01-24

    Application Number : 74255

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Impax Laboratories

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    Impax Laboratories

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;40MG

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    Approval Date : 2007-03-30

    Application Number : 77833

    Regulatory Info : DISCN

    Registration Country : USA

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    Impax Laboratories

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;80MG

    Packaging :

    Approval Date : 2007-03-30

    Application Number : 77833

    Regulatory Info : DISCN

    Registration Country : USA

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    Natco Pharma

    India
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    Natco Pharma

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;40MG

    Packaging :

    Approval Date : 2008-02-15

    Application Number : 78688

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Natco Pharma

    India
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    Natco Pharma

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : NADOLOL AND BENDROFLUMETHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;80MG

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    Approval Date : 2008-02-15

    Application Number : 78688

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Pfizer Inc

    U.S.A
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    Pfizer Inc

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : CORZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1983-05-25

    Application Number : 18647

    Regulatory Info : DISCN

    Registration Country : USA

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    Pfizer Inc

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    Pfizer Inc

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    BENDROFLUMETHIAZIDE; NADOLOL

    Brand Name : CORZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1983-05-25

    Application Number : 18647

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Rising Pharmaceuticals Inc

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    Rising Pharmaceuticals Inc

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 1993-10-31

    Application Number : 74172

    Regulatory Info : RX

    Registration Country : USA

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    18

    Rising Pharmaceuticals Inc

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 1993-10-31

    Application Number : 74172

    Regulatory Info : RX

    Registration Country : USA

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    19

    Rising Pharmaceuticals Inc

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    Rising Pharmaceuticals Inc

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

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    Approval Date : 1993-10-31

    Application Number : 74172

    Regulatory Info : RX

    Registration Country : USA

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    20

    Sandoz B2B

    Switzerland
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    Sandoz B2B

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 1995-11-09

    Application Number : 74501

    Regulatory Info : RX

    Registration Country : USA

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    Sandoz B2B

    Switzerland
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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 1995-11-09

    Application Number : 74501

    Regulatory Info : RX

    Registration Country : USA

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    Sandoz B2B

    Switzerland
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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 1995-11-09

    Application Number : 74501

    Regulatory Info : RX

    Registration Country : USA

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    23

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Teva Pharmaceutical Industries

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 1994-08-31

    Application Number : 74368

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Teva Pharmaceutical Industries

    Israel
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    Teva Pharmaceutical Industries

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    Regulatory Info : DISCN

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    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 120MG

    Packaging :

    Approval Date : 1994-08-31

    Application Number : 74368

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
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    Virtual Booth Virtual Booth
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : NADOLOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 160MG

    Packaging :

    Approval Date : 1994-08-31

    Application Number : 74368

    Regulatory Info : DISCN

    Registration Country : USA

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    Virtual Booth

    Digital Content

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    26

    US WorldMeds

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

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : CORGARD

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    27

    US WorldMeds

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

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : CORGARD

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    US WorldMeds

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

    US WorldMeds

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : CORGARD

    Dosage Form : TABLET;ORAL

    Dosage Strength : 120MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    US WorldMeds

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

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : CORGARD

    Dosage Form : TABLET;ORAL

    Dosage Strength : 160MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    30

    US WorldMeds

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

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    Brand Name : CORGARD

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 1986-10-28

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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