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    Looking for Controlled & Modified Release? Find poly l lactic acid for stability, solubility & bioavailability enhancement on PharmaCompass.

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    Poly L Lactic Acid

    INACTIVE PHARMA INGREDIENTS

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    Nomisma Healthcare

    PLLA-PEG

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    Fi Europe 2024
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    PLLA

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    Dosage Form : Tablet

    Grade : Oral, Parenteral

    Brand Name : PLLA

    Application : Controlled & Modified Release

    Excipient Details : PLLA (Poly-L-lactide) is different polymer developed to formulate polymeric nanoparticles. PLLA is biodegradable & biocompatible, and it is approved by FDA and European Medicine Agency for parenteral administration.

    Pharmacopoeia Ref : NA

    Technical Specs : Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group

    Ingredient(s) : Poly L Lactide

    Dosage Form : Tablet

    Grade : Oral, Parenteral

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    • 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.

    Ingredient(s) : Poly L Lactide

    Dosage Form : Tablet

    Category : Controlled & Modified Release

    Brand : PLLA

    Applications : PLLA (Poly-L-lactide) is different polymer developed to formulate polymeric nanoparticles. PLLA is biodegradable & biocompatible, and it is approved by FDA and European Medicine Agency for parenteral administration.

    Pharmacopoeia Ref : NA

    Technical Specs : Nano-particles, ultrapure, low-monomer & powder grades, viscosity range from 0.08 to 1.4 dL/g, ester/acid end group

    Grade : Oral, Parenteral

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