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    Looking for Controlled & Modified Release? Find Controlled & Modified Release Agents used in Duloxetine Hydrochloride to address drug delivery challenges on PharmaCompass.

    SPI Pharma has been solving formulation challenges using superior functional materials.

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    High-quality raw materials and custom blends for pharma, biopharma, nutrition, veterinary, and cosmetics worldwide.

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    Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

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    Gangwal Healthcare is powered by innovation, driving health, wellness & healing.

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    Boai NKY Pharmaceuticals Ltd. is one of the largest global PVP suppliers.

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    Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.

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    Duloxetine Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    PATENTS & EXCLUSIVITIES

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    $ API Ref.Price (USD/KG) : 215Xls

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    01 3Evonik

    02 5Nanjing Well Pharmaceutical

    03 2Actylis

    04 2Aeon Procare

    05 2Alcedo Pharmachem

    06 36BASF

    07 4Finar

    08 2Gangwal Chemicals

    09 3Ideal Cures

    10 9Kerry

    11 1Kima Chemical

    12 1Lonza Capsugel

    13 2Nomisma Healthcare

    14 2The Dow Chemical Company

    15 5Vertellus

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    PharmaCompass

    01

    Evonik

    Germany
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    CPhI WW Frankfurt
    Booth #5.1A24
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothEvonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

    Dosage Form : Capsule, Granule / Pellet, Tablet

    Grade : Oral

    Brand Name : EUDRAGIT® L 100-55

    Application : Coating Systems & Additives, Controlled & Modified Release, Solubilizers

    Excipient Details : EUDRAGIT® L 100-55 (powder) is used in delayed release coatings to enhance solubility of poorly soluble drugs such as tablets, capsules & granules.

    Pharmacopoeia Ref : NA

    Technical Specs : NA

    Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer

    Dosage Form : Capsule, Granule / Pellet, Tablet

    Grade : Oral

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    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothEvonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!

    Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer

    Dosage Form : Capsule, Granule / Pellet, Tablet

    Category : Coating Systems & Additives, Controlled & Modified Release, Solubilizers

    Brand : EUDRAGIT® L 100-55

    Applications : EUDRAGIT® L 100-55 (powder) is used in delayed release coatings to enhance solubility of poorly soluble drugs such as tablets, capsules & granules.

    Pharmacopoeia Ref : NA

    Technical Specs : NA

    Grade : Oral

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    EUDRAGIT® L 100-55

    Excipients Web Link

    Market Place

    Digital Content

    Virtual Booth

    02

    Nanjing Well Pharmaceutical

    China
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    CPhI WW Frankfurt
    Booth #12.1G60
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothNanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

    Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels

    Grade : Parenteral, Topical, Oral

    Brand Name : Polyethylene Glycol 400

    Application : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical

    Excipient Details : PEG 400 is used as a suspending agent, stabilizer, plasticizer and filler in OSDs, liquids & semi-solids and as a solvent for parenteral formulations.

    Pharmacopoeia Ref : ChP/USP/EP

    Technical Specs : NA

    Ingredient(s) : Polyethylene Glycol 400

    Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels

    Grade : Parenteral, Topical, Oral

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    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothNanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

    Ingredient(s) : Polyethylene Glycol 400

    Dosage Form : Cream / Lotion / Ointment, Gel, Injectable / Parenteral, Softgel Capsule, Softgels

    Category : Fillers, Diluents & Binders, Film Formers & Plasticizers, Parenteral, Surfactant & Foaming Agents, Thickeners and Stabilizers, Topical

    Brand : POLYETHYLENE GLYCOL 400

    Applications : PEG 400 is used as a suspending agent, stabilizer, plasticizer and filler in OSDs, liquids & semi-solids and as a solvent for parenteral formulations.

    Pharmacopoeia Ref : ChP/USP/EP

    Technical Specs : NA

    Grade : Parenteral, Topical, Oral

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    Nanjing Well Polyethylene Glycol 400 NF

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    03

    BASF

    KOLLIDON SR

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    OTS 2025
    Not Confirmed

    BASF

    Germany
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    OTS 2025
    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.

    Dosage Form : Capsule, Tablet, Topical Film, Transdermal Patch

    Grade :

    Brand Name : Kollidon SR

    Application : Controlled & Modified Release, Direct Compression, Granulation

    Excipient Details : For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

    Pharmacopoeia Ref : Ph. Eur., USP-NF, JP-JPE: 80 %...

    Technical Specs :

    Ingredient(s) : Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone

    Dosage Form : Capsule, Tablet, Topical Film, Transdermal Patch

    Grade :

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    • WHO-GMP
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    Ingredient(s) : Hydrated Silica, Lauryl Sulfate, Polyvinyl Acetate, Povidone

    Dosage Form : Capsule, Tablet, Topical Film, Transdermal Patch

    Category : Controlled & Modified Release, Direct Compression, Granulation

    Brand : KOLLIDON SR

    Applications : For non-erodible matrices using direct compression, Controlled release matrix. Matrix former in transdermal patches and topical films.

    Pharmacopoeia Ref : Ph. Eur., USP-NF, JP-JPE: 80 % Polyvinyl acetate and 19 % povidone, 0.8 % lauryl sulfate & 0.2 % silica (4:1)

    Technical Specs : Not Available

    Grade : Not Available

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    Excipients Web Link

    Market Place

    Digital Content

    Virtual Booth

    04

    Nomisma Healthcare

    PLLA-PEG

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    OTS 2025
    Not Confirmed

    05

    Aeon Procare

    TALC

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    OTS 2025
    Not Confirmed

    06

    Nomisma Healthcare

    PLGA-PEG

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    OTS 2025
    Not Confirmed

    Nomisma Healthcare

    India
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    OTS 2025
    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.

    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 Excipient

    Dosage Form : Tablet

    Grade : Oral, Parenteral

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

    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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    Excipients Web Link

    Market Place

    Digital Content

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    07

    Alcedo Pharmachem

    LUMACRIL L-100D 55

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    OTS 2025
    Not Confirmed

    Alcedo Pharmachem

    India
    arrow
    OTS 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Dosage Form : Capsule, Tablet

    Grade : Oral

    Brand Name : Lumacril L-100D 55

    Application : Coating Systems & Additives, Controlled & Modified Release, Solubilizers

    Excipient Details : Lumacril L-100D 55 is an anionic copolymer used in delayed & sustained release coatings to enhance solubility for poorly soluble drugs in OSDs.

    Pharmacopoeia Ref : USP-NF, Ph.Eur, BP, JP

    Technical Specs : NA

    Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer

    Dosage Form : Capsule, Tablet

    Grade : Oral

    arrow
    • 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.

    Ingredient(s) : Methacrylic Acid - Ethyl Acrylate Copolymer

    Dosage Form : Capsule, Tablet

    Category : Coating Systems & Additives, Controlled & Modified Release, Solubilizers

    Brand : LUMACRIL L-100D 55

    Applications : Lumacril L-100D 55 is an anionic copolymer used in delayed & sustained release coatings to enhance solubility for poorly soluble drugs in OSDs.

    Pharmacopoeia Ref : USP-NF, Ph.Eur, BP, JP

    Technical Specs : NA

    Grade : Oral

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    blank

    Excipients Web Link

    Market Place

    Digital Content

    Virtual Booth

    08

    Ideal Cures

    ECOPOL L 30 D-55

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    OTS 2025
    Not Confirmed

    09

    Finar

    POLYETHYLENE GLYCOL 400

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    OTS 2025
    Not Confirmed

    10

    Ideal Cures

    ECOPOL L100 55

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    OTS 2025
    Not Confirmed