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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    SECOBARBITAL SODIUM

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    01 1Actavis Inc

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    05 1ELKINS SINN

    06 5Eli Lilly

    07 1HALSEY

    08 1IVAX Pharmaceuticals Inc

    09 1KV Pharmaceutical

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    01

    Actavis Inc

    Ireland
    Fi Europe 2024
    Not Confirmed
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    Actavis Inc

    Ireland
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85792

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Anabolic Laboratories

    U.S.A
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    Anabolic Laboratories

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    Brand Name : SECOBARBITAL SODIUM

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    Approval Date : 1982-01-01

    Application Number : 84422

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    03

    Barr Laboratories

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    Brand Name : SECOBARBITAL SODIUM

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    Approval Date : 1982-01-01

    Application Number : 84225

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    04

    Bausch Health

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    Brand Name : SECOBARBITAL SODIUM

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    Approval Date : 1982-01-01

    Application Number : 85477

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    05

    Bausch Health

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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

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    Dosage Strength : 50MG

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    Approval Date : 1983-10-03

    Application Number : 86101

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    Bausch Health

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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

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    Dosage Strength : 100MG

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    Approval Date : 1983-10-03

    Application Number : 86101

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    07

    Eli Lilly

    U.S.A
    Fi Europe 2024
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    Fi Europe 2024
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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML **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 : 7392

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Eli Lilly

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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86530

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Eli Lilly

    U.S.A
    Fi Europe 2024
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 60MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86530

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Eli Lilly

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 120MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86530

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Eli Lilly

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Eli Lilly

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    Fi Europe 2024
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    SECOBARBITAL SODIUM

    Brand Name : SECONAL SODIUM

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86530

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    everyLIFE Technologies

    United Kingdom
    Fi Europe 2024
    Not Confirmed
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    everyLIFE Technologies

    United Kingdom
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    Fi Europe 2024
    Not Confirmed
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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85895

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    IVAX Pharmaceuticals Inc

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    IVAX Pharmaceuticals Inc

    U.S.A
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85869

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    KV Pharmaceutical

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    KV Pharmaceutical

    U.S.A
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85285

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Lannett Company, Inc.

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85903

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Lannett Company, Inc.

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Lannett Company, Inc.

    U.S.A
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    Fi Europe 2024
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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85909

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Perrigo Company plc

    Ireland
    Fi Europe 2024
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    Perrigo Company plc

    Ireland
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    Fi Europe 2024
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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84561

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Pfizer Inc

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    Fi Europe 2024
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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84762

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    PUREPAC PHARM

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    PUREPAC PHARM

    U.S.A
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85867

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    West-ward Pharmaceutical Corp

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    West-ward Pharmaceutical Corp

    U.S.A
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    Fi Europe 2024
    Not Confirmed
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84926

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Wyeth Pharmaceuticals Inc

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

    U.S.A
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83262

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Wyeth Pharmaceuticals Inc

    U.S.A
    Fi Europe 2024
    Not Confirmed
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    Wyeth Pharmaceuticals Inc

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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86390

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    ELKINS SINN

    Country
    Fi Europe 2024
    Not Confirmed
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    ELKINS SINN

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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 100MG/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83281

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    HALSEY

    Country
    Fi Europe 2024
    Not Confirmed
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    HALSEY

    Country
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    Fi Europe 2024
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84676

    Regulatory Info : DISCN

    Registration Country : USA

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    WHITEWORTH TOWN PLSN

    Country
    Fi Europe 2024
    Not Confirmed
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    WHITEWORTH TOWN PLSN

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    Fi Europe 2024
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    Regulatory Info : DISCN

    Registration Country : USA

    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85798

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    VITARINE

    Country
    Fi Europe 2024
    Not Confirmed
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    VITARINE

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    Fi Europe 2024
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

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    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85898

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    VITARINE

    Country
    Fi Europe 2024
    Not Confirmed
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    VITARINE

    Country
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    Fi Europe 2024
    Not Confirmed
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    • EDQM
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : DISCN

    Registration Country : USA

    SECOBARBITAL SODIUM

    Brand Name : SECOBARBITAL SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86273

    Regulatory Info : DISCN

    Registration Country : USA

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