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    Brand Name : PHENTERMINE HYDROCHL...

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    RLD : No

    TE Code : AB

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Actavis Inc

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : PHENTERMINE HYDROCHLORID...

    Dosage Strength : EQ 11.25MG BASE;69MG

    Approval Date : 2024-06-25

    Application Number : 204982

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
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    RLD : No

    TE Code : AB

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Actavis Inc

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : PHENTERMINE HYDROCHLORID...

    Dosage Strength : EQ 3.75MG BASE;23MG

    Approval Date : 2024-06-25

    Application Number : 204982

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
    BePharma
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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
    BePharma
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    RLD : No

    TE Code : AB

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Actavis Inc

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : PHENTERMINE HYDROCHLORID...

    Dosage Strength : EQ 15MG BASE;92MG

    Approval Date : 2024-06-25

    Application Number : 204982

    RX/OTC/DISCN : RX

    RLD : No

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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
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    Brand Name : PHENTERMINE HYDROCHL...

    Ireland
    BePharma
    Not Confirmed
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    • 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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    RLD : No

    TE Code : AB

    PHENTERMINE HYDROCHLORIDE; TOPIRAMATE

    Actavis Inc

    Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

    Proprietary Name : PHENTERMINE HYDROCHLORID...

    Dosage Strength : EQ 7.5MG BASE;46MG

    Approval Date : 2024-06-25

    Application Number : 204982

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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