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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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    Jai Radhe Sales is your partner for all your sourcing needs.

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    xyz-pharma-m-2024-10-07

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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

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    xyz-pharma-m-2024-10-07

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    Butabarbital

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 1ALPHARMA US PHARMS

    02 1BUNDY

    03 3HALSEY

    04 2HIKMA

    05 2IVAX SUB TEVA PHARMS

    06 4LANNETT

    07 2MARSHALL PHARMA

    08 1MEDA PHARMS

    09 4MEDPOINTE PHARM HLC

    10 4NORVIUM BIOSCIENCE

    11 4SANDOZ

    12 4SOLVAY

    13 2TEVA

    14 2WATSON LABS

    15 2WHITEWORTH TOWN PLSN

    16 1WOCKHARDT

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    01

    IVAX SUB TEVA PHARMS

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    IVAX SUB TEVA PHARMS

    U.S.A
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    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : SODIUM BUTABARBITAL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Approval Date : 1982-01-01

    Application Number : 83484

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    SOLVAY

    Belgium
    Pharmtech & Ingredients
    Not Confirmed
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    SOLVAY

    Belgium
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    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTABARBITAL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 16.2MG

    Approval Date : 1982-01-01

    Application Number : 83606

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    NORVIUM BIOSCIENCE

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    NORVIUM BIOSCIENCE

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    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTISOL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 793

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    NORVIUM BIOSCIENCE

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
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    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTISOL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 793

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    NORVIUM BIOSCIENCE

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
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    Pharmtech & Ingredients
    Not Confirmed
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    • EDQM
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    RLD : Yes

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTISOL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 30MG

    Approval Date : 1982-01-01

    Application Number : 793

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    06

    NORVIUM BIOSCIENCE

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    NORVIUM BIOSCIENCE

    Country
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    Pharmtech & Ingredients
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTISOL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 793

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    WHITEWORTH TOWN PLSN

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    WHITEWORTH TOWN PLSN

    Country
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    Pharmtech & Ingredients
    Not Confirmed
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTABARBITAL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Approval Date : 1982-01-01

    Application Number : 83325

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    WHITEWORTH TOWN PLSN

    Country
    Pharmtech & Ingredients
    Not Confirmed
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    WHITEWORTH TOWN PLSN

    Country
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : BUTABARBITAL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 30MG

    Approval Date : 1982-01-01

    Application Number : 83337

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    MARSHALL PHARMA

    Country
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    MARSHALL PHARMA

    Country
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : SODIUM BUTABARBITAL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 16.2MG

    Approval Date : 1982-01-01

    Application Number : 83524

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    MARSHALL PHARMA

    Country
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    MARSHALL PHARMA

    Country
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • 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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    RLD : No

    TE Code :

    BUTABARBITAL SODIUM

    Brand Name : SODIUM BUTABARBITAL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 32.4MG

    Approval Date : 1982-01-01

    Application Number : 83858

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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