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    Looking for Pharmaceutical Excipients offered by Nomisma Healthcare? Find Poly DL Lactic Acid based excipient solutions to address drug delivery challenges on PharmaCompass.

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    Salicylic Acid

    ACTIVE PHARMA INGREDIENTS

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    $ API Ref.Price (USD/KG) : 4Xls

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    Nomisma Healthcare

    PLLA-PEG

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    Fi Europe 2024
    Not Confirmed

    02

    Nomisma Healthcare

    PLGA-PEG

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    Fi Europe 2024
    Not Confirmed

    Nomisma Healthcare

    India
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    Fi Europe 2024
    Not Confirmed
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    Dosage Form : Tablet

    Grade : Oral, Parenteral

    Brand Name : PLGA-PEG

    Application : Controlled & Modified Release

    Excipient Details : PLGA-PEG is used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

    Pharmacopoeia Ref : NA

    Technical Specs : Nano-particles, ultrapure, low-monomer & powder grades.

    Ingredient(s) : Poly-DL-Lactic-co-Glycolic Acid, Polyethylene Glycol Excipients

    Dosage Form : Tablet

    Grade : Oral, Parenteral

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    • WHO-GMP
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    Ingredient(s) : Poly-DL-Lactic-co-Glycolic Acid, Polyethylene Glycol Excipients

    Dosage Form : Tablet

    Category : Controlled & Modified Release

    Brand : PLGA-PEG

    Applications : PLGA-PEG is used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs.

    Pharmacopoeia Ref : NA

    Technical Specs : Nano-particles, ultrapure, low-monomer & powder grades.

    Grade : Oral, Parenteral

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    03

    Nomisma Healthcare

    PDLLA

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    Fi Europe 2024
    Not Confirmed

    Nomisma Healthcare

    India
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    Fi Europe 2024
    Not Confirmed
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    Dosage Form : Injectable / Parenteral, Tablet

    Grade : Oral, Parenteral

    Brand Name : PDLLA

    Application : Controlled & Modified Release, Parenteral

    Excipient Details : PDLLA (Poly-DL-lactide) is different polymers developed to formulate polymeric nanoparticles. PDLLA is biodegradable & biocompatible, and it has the FDA and EMA approval in drug delivery systems 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 DL Lactide

    Dosage Form : Injectable / Parenteral, Tablet

    Grade : Oral, Parenteral

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    • EDQM
    • WHO-GMP
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    Ingredient(s) : Poly DL Lactide

    Dosage Form : Injectable / Parenteral, Tablet

    Category : Controlled & Modified Release, Parenteral

    Brand : PDLLA

    Applications : PDLLA (Poly-DL-lactide) is different polymers developed to formulate polymeric nanoparticles. PDLLA is biodegradable & biocompatible, and it has the FDA and EMA approval in drug delivery systems 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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    Excipients Web Link

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