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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.https://marketing.lgmpharma.com/LGM-CDMO

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    Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

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    Mertiatide

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    01 1ROTOP Pharmaka GmbH

    02 2Rotop Pharmaka Gmbh

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    ROTOP Pharmaka GmbH

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    euroPLX 90 Lisbon
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    ROTOP Pharmaka GmbH

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    euroPLX 90 Lisbon
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    Regulatory Info : Marketed

    Registration Country : Norway

    Mertiatide

    Brand Name : Nephromag

    Dosage Form : Radiopharmaceutical Preparation Kits

    Dosage Strength : 0.2mg/2.5ml

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    Approval Date :

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    Regulatory Info : Marketed

    Registration Country : Norway

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    02

    Rotop Pharmaka Gmbh

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    euroPLX 90 Lisbon
    Not Confirmed
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    Rotop Pharmaka Gmbh

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    euroPLX 90 Lisbon
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Authorized

    Registration Country : Spain

    Mertiatida

    Brand Name : Nephromag

    Dosage Form : Reagent Kit For Pharmaceutical Preparation

    Dosage Strength : 200MCG

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    Approval Date : 11-12-2007

    Application Number : 69466

    Regulatory Info : Authorized

    Registration Country : Spain

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    03

    Rotop Pharmaka Gmbh

    Country
    euroPLX 90 Lisbon
    Not Confirmed
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    Rotop Pharmaka Gmbh

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    euroPLX 90 Lisbon
    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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    Regulatory Info : Prescription

    Registration Country : Denmark

    Mertiatid

    Brand Name : Nephromag

    Dosage Form : Radiopharmaceutical

    Dosage Strength : 0.2mg

    Packaging :

    Approval Date : 15-12-2016

    Application Number : 28125621315

    Regulatory Info : Prescription

    Registration Country : Denmark

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.