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    Tetracycline Phosphate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

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    01

    BRISTOL

    United Kingdom
    Pharmtech & Ingredients
    Not Confirmed
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    United Kingdom
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    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 50212

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    BRISTOL

    United Kingdom
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    BRISTOL

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

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 50212

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    03

    BRISTOL

    United Kingdom
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    BRISTOL

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    • EDQM
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    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 61653

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    04

    BRISTOL

    United Kingdom
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    BRISTOL

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    Pharmtech & Ingredients
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    • EDQM
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    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 61653

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

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    Website

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    05

    BRISTOL

    United Kingdom
    Pharmtech & Ingredients
    Not Confirmed
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    BRISTOL

    United Kingdom
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    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 61653

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    06

    BRISTOL

    United Kingdom
    Pharmtech & Ingredients
    Not Confirmed
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    BRISTOL

    United Kingdom
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 61889

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

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    Digital Content

    Website

    Corporate PDF

    07

    BRISTOL

    United Kingdom
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    BRISTOL

    United Kingdom
    arrow
    Pharmtech & Ingredients
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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.
    Post an Enquiry Post an Enquiry
    Flag United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    TETRACYCLINE PHOSPHATE COMPLEX

    Brand Name : TETREX

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG HYDROCHLORIDE

    Approval Date : 1982-01-01

    Application Number : 61889

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF